chr11:5227159:G>C Detail (hg38) (HBB, LOC106099062, LOC107133510)

Information

Genome

Assembly Position
hg19 chr11:5,248,389-5,248,389 View the variant detail on this assembly version.
hg38 chr11:5,227,159-5,227,159

HGVS

Type Transcript Protein
RefSeq
Ensemble ENST00000647020.1:c.-138C>G
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Uncertain significance
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 2019-11-25 no assertion criteria provided beta thalassemia germline Detail
Uncertain significance 2022-12-07 criteria provided, single submitter not provided unknown Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.287 alpha-Thalassemia NA CLINVAR Detail
0.244 Beta thalassemia intermedia NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000518.4(HBB):c.-138C>G AND beta Thalassemia ClinVar Detail
NM_000518.4(HBB):c.-138C>G AND not provided ClinVar Detail
NA DisGeNET 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
rs33944208 dbSNP
Genome
hg38
Position
chr11:5,227,159-5,227,159
Variant Type
snv
Reference Allele
G
Alternative Allele
C
Genome browser