Canonical Allele Identifier: CA3710755

Gene: HLA-C

Linked Data

• dbSNP Id: rs1065406
• ExAC: 6:31239049 G / T
• gnomAD v2: 6-31239049-G-T
• gnomAD v3: 6-31271272-G-T
• gnomAD v4: 6-31271272-G-T
• MyVariant Identifiers: chr6:g.31239049G>T (hg19) ; chr6:g.31271272G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271272G>T , CM000668.2:g.31271272G>T	GRCh38
NC_000006.11:g.31239049G>T , CM000668.1:g.31239049G>T	GRCh37
NC_000006.10:g.31347028G>T	NCBI36
NG_029422.2:g.5860C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.420C>A MANE Select	ENSP00000365402.5:p.Ser140=
ENST00000376228.9:c.420C>A	ENSP00000365402.5:p.Ser140=
ENST00000376237.8:c.*7C>A	ENSP00000365412.4:n.*7C>A
ENST00000383329.7:c.420C>A	ENSP00000372819.3:p.Ser140=
ENST00000415537.1:c.418C>A
ENST00000484378.1:n.689C>A
ENST00000487245.5:n.779C>A
ENST00000495835.1:n.609C>A
NM_002117.5:c.420C>A	NP_002108.4:p.Ser140=
NM_002117.6:c.420C>A MANE Select	NP_002108.4:p.Ser140=