Canonical Allele Identifier: CA363321891
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31270360-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270360T>C , CM000668.2:g.31270360T>C GRCh38
NC_000006.11:g.31238137T>C , CM000668.1:g.31238137T>C GRCh37
NC_000006.10:g.31346116T>C NCBI36
NG_029422.2:g.6772A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.745A>G MANE Select ENSP00000365402.5:p.Thr249Ala
ENST00000376228.9:c.745A>G ENSP00000365402.5:p.Thr249Ala
ENST00000376237.8:c.*332A>G ENSP00000365412.4:n.*332A>G
ENST00000383329.7:c.745A>G ENSP00000372819.3:p.Thr249Ala
ENST00000415537.1:c.665-29A>G
ENST00000470363.5:n.63A>G
ENST00000487245.5:n.1104A>G
ENST00000495835.1:n.934A>G
NM_002117.5:c.745A>G NP_002108.4:p.Thr249Ala
NM_002117.6:c.745A>G MANE Select NP_002108.4:p.Thr249Ala