Canonical Allele Identifier: CA136867365

Gene: HLA-C

Linked Data

• dbSNP Id: rs281860472
• gnomAD v3: 6-31271263-G-T
• gnomAD v4: 6-31271263-G-T
• MyVariant Identifiers: chr6:g.31239040G>T (hg19) ; chr6:g.31271263G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271263G>T , CM000668.2:g.31271263G>T	GRCh38
NC_000006.11:g.31239040G>T , CM000668.1:g.31239040G>T	GRCh37
NC_000006.10:g.31347019G>T	NCBI36
NG_029422.2:g.5869C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.429C>A MANE Select	ENSP00000365402.5:p.Asp143Glu
ENST00000376228.9:c.429C>A	ENSP00000365402.5:p.Asp143Glu
ENST00000376237.8:c.*16C>A	ENSP00000365412.4:n.*16C>A
ENST00000383329.7:c.429C>A	ENSP00000372819.3:p.Asp143Glu
ENST00000415537.1:c.427C>A
ENST00000484378.1:n.698C>A
ENST00000487245.5:n.788C>A
ENST00000495835.1:n.618C>A
NM_002117.5:c.429C>A	NP_002108.4:p.Asp143Glu
NM_002117.6:c.429C>A MANE Select	NP_002108.4:p.Asp143Glu