Canonical Allele Identifier: CA3710442

Gene: HLA-C

Linked Data

• dbSNP Id: rs17886232
• ExAC: 6:31237965 G / T
• gnomAD v4: 6-31270188-G-T
• MyVariant Identifiers: chr6:g.31237965G>T (hg19) ; chr6:g.31270188G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270188G>T , CM000668.2:g.31270188G>T	GRCh38
NC_000006.11:g.31237965G>T , CM000668.1:g.31237965G>T	GRCh37
NC_000006.10:g.31345944G>T	NCBI36
NG_029422.2:g.6944C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.895+22C>A MANE Select	ENSP00000365402.5:n.895+22C>A
ENST00000376228.9:c.895+22C>A	ENSP00000365402.5:n.895+22C>A
ENST00000376237.8:c.*482+22C>A	ENSP00000365412.4:n.*482+22C>A
ENST00000383329.7:c.895+22C>A	ENSP00000372819.3:n.895+22C>A
ENST00000470363.5:n.213+22C>A
ENST00000487245.5:n.1254+22C>A
NM_002117.5:c.895+22C>A	NP_002108.4:n.895+22C>A
NM_002117.6:c.895+22C>A MANE Select	NP_002108.4:n.895+22C>A