Canonical Allele Identifier: CA565887218

Gene: HLA-G

Linked Data

• dbSNP Id: rs1238734285
• gnomAD v2: 6-29798623-A-G
• gnomAD v4: 6-29830846-A-G
• MyVariant Identifiers: chr6:g.29798623A>G (hg19) ; chr6:g.29830846A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29830846A>G , CM000668.2:g.29830846A>G	GRCh38
NC_000006.11:g.29798623A>G , CM000668.1:g.29798623A>G	GRCh37
NC_000006.10:g.29906602A>G	NCBI36
NG_029039.1:g.8868A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360323.11:c.*107A>G MANE Select	ENSP00000353472.6:n.*107A>G
ENST00000360323.10:c.*107A>G	ENSP00000353472.6:n.*107A>G
ENST00000376815.3:c.572A>G	ENSP00000366011.3:n.572A>G
ENST00000376818.7:c.848A>G	ENSP00000366014.3:n.848A>G
ENST00000376828.6:c.*107A>G	ENSP00000366024.2:n.*107A>G
ENST00000428701.5:c.*107A>G	ENSP00000412927.1:n.*107A>G
ENST00000478355.5:n.1246A>G
ENST00000478519.5:c.896A>G	ENSP00000436375.1:n.896A>G
NM_002127.5:c.*107A>G	NP_002118.1:n.*107A>G
NM_001363567.1:c.*107A>G	NP_001350496.1:n.*107A>G
XM_017010817.1:c.*107A>G	XP_016866306.1:n.*107A>G
NM_001363567.2:c.*107A>G	NP_001350496.1:n.*107A>G
NM_001384280.1:c.*107A>G	NP_001371209.1:n.*107A>G
NM_001384290.1:c.*107A>G MANE Select	NP_001371219.1:n.*107A>G
NM_002127.6:c.*107A>G	NP_002118.1:n.*107A>G