Canonical Allele Identifier: CA363322736

Gene: HLA-C

Linked Data

• dbSNP Id: rs2113906877
• gnomAD v4: 6-31270458-T-A
• MyVariant Identifiers: chr6:g.31238235T>A (hg19) ; chr6:g.31270458T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270458T>A , CM000668.2:g.31270458T>A	GRCh38
NC_000006.11:g.31238235T>A , CM000668.1:g.31238235T>A	GRCh37
NC_000006.10:g.31346214T>A	NCBI36
NG_029422.2:g.6674A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.647A>T MANE Select	ENSP00000365402.5:p.His216Leu
ENST00000376228.9:c.647A>T	ENSP00000365402.5:p.His216Leu
ENST00000376237.8:c.*234A>T	ENSP00000365412.4:n.*234A>T
ENST00000383329.7:c.647A>T	ENSP00000372819.3:p.His216Leu
ENST00000415537.1:c.645A>T
ENST00000487245.5:n.1006A>T
ENST00000495835.1:n.836A>T
NM_002117.5:c.647A>T	NP_002108.4:p.His216Leu
NM_002117.6:c.647A>T MANE Select	NP_002108.4:p.His216Leu