HSH2D hematopoietic SH2 domain containing

Information
Symbol
HSH2D
Type
protein-coding
Description
hematopoietic SH2 domain containing
Entrez Gene ID
84941
Genome
hg19
Position
chr19:16,244,838-16,269,381
Genome
hg38
Position
chr19:16,134,028-16,158,570
MIM
608349 OMIM
HGNC
HGNC:24920 HGNC
Ensembl
ENSG00000196684 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Uncertain significance 0 34
Ranking
ClinVar
0
0
0
38
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM ALX
SYNONYM HSH2
MIM 608349 OMIM
HGNC HGNC:24920 HGNC
Ensembl ENSG00000196684 Ensembl
AllianceGenome HGNC:24920
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000616645.4 hg38 chr19 16,134,028 16,158,570 24,543
ENST00000613986.4 hg38 chr19 16,143,685 16,158,575 14,891
ENST00000616645.4 hg19 chr19 16,244,838 16,269,381 24,544
ENST00000613986.4 hg19 chr19 16,254,495 16,269,386 14,892
Genome browser