Canonical Allele Identifier: CA136861095
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs944486922
MyVariant Identifiers: chr6:g.31236740A>T (hg19) chr6:g.31268963A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268963A>T , CM000668.2:g.31268963A>T GRCh38
NC_000006.11:g.31236740A>T , CM000668.1:g.31236740A>T GRCh37
NC_000006.10:g.31344719A>T NCBI36
NG_029422.2:g.8169T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*206T>A MANE Select ENSP00000365402.5:n.*206T>A
ENST00000376228.9:c.*206T>A ENSP00000365402.5:n.*206T>A
ENST00000376237.8:c.*894T>A ENSP00000365412.4:n.*894T>A
ENST00000383329.7:c.*206T>A ENSP00000372819.3:n.*206T>A
ENST00000466892.5:n.540T>A
ENST00000470363.5:n.1065T>A
ENST00000487245.5:n.1666T>A
NM_002117.5:c.*206T>A NP_002108.4:n.*206T>A
NM_002117.6:c.*206T>A MANE Select NP_002108.4:n.*206T>A
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