Canonical Allele Identifier: CA363322862

Gene: HLA-C

Linked Data

• gnomAD v3: 6-31270476-T-A
• gnomAD v4: 6-31270476-T-A
• MyVariant Identifiers: chr6:g.31238253T>A (hg19) ; chr6:g.31270476T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270476T>A , CM000668.2:g.31270476T>A	GRCh38
NC_000006.11:g.31238253T>A , CM000668.1:g.31238253T>A	GRCh37
NC_000006.10:g.31346232T>A	NCBI36
NG_029422.2:g.6656A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.629A>T MANE Select	ENSP00000365402.5:p.Lys210Met
ENST00000376228.9:c.629A>T	ENSP00000365402.5:p.Lys210Met
ENST00000376237.8:c.*216A>T	ENSP00000365412.4:n.*216A>T
ENST00000383329.7:c.629A>T	ENSP00000372819.3:p.Lys210Met
ENST00000415537.1:c.627A>T
ENST00000487245.5:n.988A>T
ENST00000495835.1:n.818A>T
NM_002117.5:c.629A>T	NP_002108.4:p.Lys210Met
NM_002117.6:c.629A>T MANE Select	NP_002108.4:p.Lys210Met