Canonical Allele Identifier: CA2677781680

Gene: HLA-G

Linked Data

• gnomAD v4: 6-29830851-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29830851A>G , CM000668.2:g.29830851A>G	GRCh38
NC_000006.11:g.29798628A>G , CM000668.1:g.29798628A>G	GRCh37
NC_000006.10:g.29906607A>G	NCBI36
NG_029039.1:g.8873A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360323.11:c.*112A>G MANE Select	ENSP00000353472.6:n.*112A>G
ENST00000360323.10:c.*112A>G	ENSP00000353472.6:n.*112A>G
ENST00000376815.3:c.577A>G	ENSP00000366011.3:n.577A>G
ENST00000376818.7:c.853A>G	ENSP00000366014.3:n.853A>G
ENST00000376828.6:c.*112A>G	ENSP00000366024.2:n.*112A>G
ENST00000428701.5:c.*112A>G	ENSP00000412927.1:n.*112A>G
ENST00000478355.5:n.1251A>G
ENST00000478519.5:c.901A>G	ENSP00000436375.1:n.901A>G
NM_002127.5:c.*112A>G	NP_002118.1:n.*112A>G
NM_001363567.1:c.*112A>G	NP_001350496.1:n.*112A>G
XM_017010817.1:c.*112A>G	XP_016866306.1:n.*112A>G
NM_001363567.2:c.*112A>G	NP_001350496.1:n.*112A>G
NM_001384280.1:c.*112A>G	NP_001371209.1:n.*112A>G
NM_001384290.1:c.*112A>G MANE Select	NP_001371219.1:n.*112A>G
NM_002127.6:c.*112A>G	NP_002118.1:n.*112A>G