Canonical Allele Identifier: CA363046923

Gene: HLA-G

Linked Data

• gnomAD v4: 6-29828683-A-G
• MyVariant Identifiers: chr6:g.29796460A>G (hg19) ; chr6:g.29828683A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29828683A>G , CM000668.2:g.29828683A>G	GRCh38
NC_000006.11:g.29796460A>G , CM000668.1:g.29796460A>G	GRCh37
NC_000006.10:g.29904439A>G	NCBI36
NG_029039.1:g.6705A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428701.6:n.588A>G
ENST00000360323.11:c.484A>G MANE Select	ENSP00000353472.6:p.Thr162Ala
ENST00000360323.10:c.484A>G	ENSP00000353472.6:p.Thr162Ala
ENST00000376815.3:c.343+367A>G	ENSP00000366011.3:n.343+367A>G
ENST00000376818.7:c.343+367A>G	ENSP00000366014.3:n.343+367A>G
ENST00000376828.6:c.499A>G	ENSP00000366024.2:p.Thr167Ala
ENST00000428701.5:c.484A>G	ENSP00000412927.1:p.Thr162Ala
ENST00000478355.5:n.484A>G
ENST00000478519.5:c.343+367A>G	ENSP00000436375.1:n.343+367A>G
NM_002127.5:c.484A>G	NP_002118.1:p.Thr162Ala
NM_001363567.1:c.499A>G	NP_001350496.1:p.Thr167Ala
XM_017010817.1:c.343+367A>G	XP_016866306.1:n.343+367A>G
XM_017010818.1:c.343+367A>G	XP_016866307.1:n.343+367A>G
XM_024446420.1:c.484A>G	XP_024302188.1:p.Thr162Ala
NM_001363567.2:c.499A>G	NP_001350496.1:p.Thr167Ala
NM_001384280.1:c.499A>G	NP_001371209.1:p.Thr167Ala
NM_001384290.1:c.484A>G MANE Select	NP_001371219.1:p.Thr162Ala
NM_002127.6:c.484A>G	NP_002118.1:p.Thr162Ala