Canonical Allele Identifier: CA2677949285
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269043-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269043A>C , CM000668.2:g.31269043A>C GRCh38
NC_000006.11:g.31236820A>C , CM000668.1:g.31236820A>C GRCh37
NC_000006.10:g.31344799A>C NCBI36
NG_029422.2:g.8089T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*126T>G MANE Select ENSP00000365402.5:n.*126T>G
ENST00000376228.9:c.*126T>G ENSP00000365402.5:n.*126T>G
ENST00000376237.8:c.*814T>G ENSP00000365412.4:n.*814T>G
ENST00000383329.7:c.*126T>G ENSP00000372819.3:n.*126T>G
ENST00000466892.5:n.460T>G
ENST00000470363.5:n.985T>G
ENST00000487245.5:n.1586T>G
NM_002117.5:c.*126T>G NP_002108.4:n.*126T>G
NM_002117.6:c.*126T>G MANE Select NP_002108.4:n.*126T>G