Canonical Allele Identifier: CA2677950115
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269806-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269806G>C , CM000668.2:g.31269806G>C GRCh38
NC_000006.11:g.31237583G>C , CM000668.1:g.31237583G>C GRCh37
NC_000006.10:g.31345562G>C NCBI36
NG_029422.2:g.7326C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1015+160C>G MANE Select ENSP00000365402.5:n.1015+160C>G
ENST00000376228.9:c.1015+160C>G ENSP00000365402.5:n.1015+160C>G
ENST00000376237.8:c.*602+160C>G ENSP00000365412.4:n.*602+160C>G
ENST00000383329.7:c.1015+160C>G ENSP00000372819.3:n.1015+160C>G
ENST00000470363.5:n.493C>G
ENST00000487245.5:n.1374+160C>G
NM_002117.5:c.1015+160C>G NP_002108.4:n.1015+160C>G
NM_002117.6:c.1015+160C>G MANE Select NP_002108.4:n.1015+160C>G