Canonical Allele Identifier: CA449789971
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31270018-T-A
MyVariant Identifiers: chr6:g.31237795T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270018T>A , CM000668.2:g.31270018T>A GRCh38
NC_000006.11:g.31237795T>A , CM000668.1:g.31237795T>A GRCh37
NC_000006.10:g.31345774T>A NCBI36
NG_029422.2:g.7114A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.963A>T MANE Select ENSP00000365402.5:p.Leu321=
ENST00000376228.9:c.963A>T ENSP00000365402.5:p.Leu321=
ENST00000376237.8:c.*550A>T ENSP00000365412.4:n.*550A>T
ENST00000383329.7:c.963A>T ENSP00000372819.3:p.Leu321=
ENST00000470363.5:n.281A>T
ENST00000487245.5:n.1322A>T
NM_002117.5:c.963A>T NP_002108.4:p.Leu321=
NM_002117.6:c.963A>T MANE Select NP_002108.4:p.Leu321=