Canonical Allele Identifier: CA3710565
Gene: HLA-C HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1050320

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270361C>T , CM000668.2:g.31270361C>T GRCh38
NC_000006.10:g.31346117C>T NCBI36
NC_000006.11:g.31238138C>T , CM000668.1:g.31238138C>T GRCh37
NG_029422.2:g.6771G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.9:c.744G>A ENSP00000365402.5:p.Gln248=
ENST00000376237.8:c.*331G>A ENSP00000365412.4:p.=
ENST00000383329.7:c.744G>A ENSP00000372819.3:p.Gln248=
ENST00000415537.1:n.665-30G>A
ENST00000470363.5:n.62G>A
ENST00000487245.5:n.1103G>A
ENST00000495835.1:n.933G>A
NM_002117.5:c.744G>A VV NP_002108.4:p.Gln248=