chr11:5226784:G>T Detail (hg38) (HBB, LOC106099062, LOC107133510)

Information

Genome

Assembly Position
hg19 chr11:5,248,014-5,248,014 View the variant detail on this assembly version.
hg38 chr11:5,226,784-5,226,784

HGVS

Type Transcript Protein
RefSeq NM_000518.4:c.108C>A NP_000509.1:p.Tyr36Ter
Ensemble ENST00000335295.4:c.108C>A ENST00000335295.4:p.Tyr36Ter
ENST00000485743.1:c.108C>A ENST00000485743.1:p.Tyr36Ter
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic
Review star
Show details
Links
Type Database ID Link
Gene MIM 141900 OMIM
HGNC 4827 HGNC
Ensembl ENSG00000244734 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic 1989-05-15 no assertion criteria provided Beta zero thalassemia germline Detail
Pathogenic 2023-09-06 criteria provided, single submitter beta thalassemia germline Detail
Pathogenic 2023-08-10 criteria provided, multiple submitters, no conflicts not provided germline unknown Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.127 beta^0^ Thalassemia NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000518.5(HBB):c.108C>A (p.Tyr36Ter) AND Beta zero thalassemia ClinVar Detail
NM_000518.5(HBB):c.108C>A (p.Tyr36Ter) AND beta Thalassemia ClinVar Detail
NM_000518.5(HBB):c.108C>A (p.Tyr36Ter) AND not provided ClinVar Detail
NA DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs33982568 dbSNP
Genome
hg38
Position
chr11:5,226,784-5,226,784
Variant Type
snv
Reference Allele
G
Alternative Allele
T
Genome browser