Canonical Allele Identifier: CA363319415

Gene: HLA-C

Linked Data

• gnomAD v4: 6-31269493-A-T
• MyVariant Identifiers: chr6:g.31237270A>T (hg19) ; chr6:g.31269493A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269493A>T , CM000668.2:g.31269493A>T	GRCh38
NC_000006.11:g.31237270A>T , CM000668.1:g.31237270A>T	GRCh37
NC_000006.10:g.31345249A>T	NCBI36
NG_029422.2:g.7639T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1048T>A MANE Select	ENSP00000365402.5:p.Cys350Ser
ENST00000376228.9:c.1048T>A	ENSP00000365402.5:p.Cys350Ser
ENST00000376237.8:c.*635T>A	ENSP00000365412.4:n.*635T>A
ENST00000383329.7:c.1066T>A	ENSP00000372819.3:p.Cys356Ser
ENST00000466892.5:n.174T>A
ENST00000470363.5:n.806T>A
ENST00000487245.5:n.1407T>A
NM_002117.5:c.1048T>A	NP_002108.4:p.Cys350Ser
NM_002117.6:c.1048T>A MANE Select	NP_002108.4:p.Cys350Ser