Canonical Allele Identifier: CA363325829
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31271208-T-C
gnomAD v4: 6-31271208-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271208T>C , CM000668.2:g.31271208T>C GRCh38
NC_000006.11:g.31238985T>C , CM000668.1:g.31238985T>C GRCh37
NC_000006.10:g.31346964T>C NCBI36
NG_029422.2:g.5924A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.484A>G MANE Select ENSP00000365402.5:p.Thr162Ala
ENST00000376228.9:c.484A>G ENSP00000365402.5:p.Thr162Ala
ENST00000376237.8:c.*71A>G ENSP00000365412.4:n.*71A>G
ENST00000383329.7:c.484A>G ENSP00000372819.3:p.Thr162Ala
ENST00000415537.1:c.482A>G
ENST00000484378.1:n.753A>G
ENST00000487245.5:n.843A>G
ENST00000495835.1:n.673A>G
NM_002117.5:c.484A>G NP_002108.4:p.Thr162Ala
NM_002117.6:c.484A>G MANE Select NP_002108.4:p.Thr162Ala