Canonical Allele Identifier: CA449789900
Gene: HLA-C HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31237744T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269967T>G , CM000668.2:g.31269967T>G GRCh38
NC_000006.11:g.31237744T>G , CM000668.1:g.31237744T>G GRCh37
NC_000006.10:g.31345723T>G NCBI36
NG_029422.2:g.7165A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1014A>C MANE Select ENSP00000365402.5:p.Ser338=
ENST00000376228.9:c.1014A>C ENSP00000365402.5:p.Ser338=
ENST00000376237.8:c.*601A>C ENSP00000365412.4:n.*601A>C
ENST00000383329.7:c.1014A>C ENSP00000372819.3:p.Ser338=
ENST00000470363.5:n.332A>C
ENST00000487245.5:n.1373A>C
NM_002117.5:c.1014A>C NP_002108.4:p.Ser338=
NM_002117.6:c.1014A>C MANE Select NP_002108.4:p.Ser338=