Canonical Allele Identifier: CA2677949619
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269312-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269312A>G , CM000668.2:g.31269312A>G GRCh38
NC_000006.11:g.31237089A>G , CM000668.1:g.31237089A>G GRCh37
NC_000006.10:g.31345068A>G NCBI36
NG_029422.2:g.7820T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1096+26T>C MANE Select ENSP00000365402.5:n.1096+26T>C
ENST00000376228.9:c.1096+26T>C ENSP00000365402.5:n.1096+26T>C
ENST00000376237.8:c.*683+26T>C ENSP00000365412.4:n.*683+26T>C
ENST00000383329.7:c.1114+26T>C ENSP00000372819.3:n.1114+26T>C
ENST00000466892.5:n.329+26T>C
ENST00000470363.5:n.854+26T>C
ENST00000487245.5:n.1455+26T>C
NM_002117.5:c.1096+26T>C NP_002108.4:n.1096+26T>C
NM_002117.6:c.1096+26T>C MANE Select NP_002108.4:n.1096+26T>C
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