Canonical Allele Identifier: CA2677949561
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269267-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269267A>T , CM000668.2:g.31269267A>T GRCh38
NC_000006.11:g.31237044A>T , CM000668.1:g.31237044A>T GRCh37
NC_000006.10:g.31345023A>T NCBI36
NG_029422.2:g.7865T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1096+71T>A MANE Select ENSP00000365402.5:n.1096+71T>A
ENST00000376228.9:c.1096+71T>A ENSP00000365402.5:n.1096+71T>A
ENST00000376237.8:c.*683+71T>A ENSP00000365412.4:n.*683+71T>A
ENST00000383329.7:c.1114+71T>A ENSP00000372819.3:n.1114+71T>A
ENST00000466892.5:n.329+71T>A
ENST00000470363.5:n.854+71T>A
ENST00000487245.5:n.1455+71T>A
NM_002117.5:c.1096+71T>A NP_002108.4:n.1096+71T>A
NM_002117.6:c.1096+71T>A MANE Select NP_002108.4:n.1096+71T>A
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