Canonical Allele Identifier: CA363046819

Gene: HLA-G

Linked Data

• gnomAD v4: 6-29828655-G-C
• MyVariant Identifiers: chr6:g.29796432G>C (hg19) ; chr6:g.29828655G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29828655G>C , CM000668.2:g.29828655G>C	GRCh38
NC_000006.11:g.29796432G>C , CM000668.1:g.29796432G>C	GRCh37
NC_000006.10:g.29904411G>C	NCBI36
NG_029039.1:g.6677G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428701.6:n.560G>C
ENST00000360323.11:c.456G>C MANE Select	ENSP00000353472.6:p.Glu152Asp
ENST00000360323.10:c.456G>C	ENSP00000353472.6:p.Glu152Asp
ENST00000376815.3:c.343+339G>C	ENSP00000366011.3:n.343+339G>C
ENST00000376818.7:c.343+339G>C	ENSP00000366014.3:n.343+339G>C
ENST00000376828.6:c.471G>C	ENSP00000366024.2:p.Glu157Asp
ENST00000428701.5:c.456G>C	ENSP00000412927.1:p.Glu152Asp
ENST00000478355.5:n.456G>C
ENST00000478519.5:c.343+339G>C	ENSP00000436375.1:n.343+339G>C
NM_002127.5:c.456G>C	NP_002118.1:p.Glu152Asp
NM_001363567.1:c.471G>C	NP_001350496.1:p.Glu157Asp
XM_017010817.1:c.343+339G>C	XP_016866306.1:n.343+339G>C
XM_017010818.1:c.343+339G>C	XP_016866307.1:n.343+339G>C
XM_024446420.1:c.456G>C	XP_024302188.1:p.Glu152Asp
NM_001363567.2:c.471G>C	NP_001350496.1:p.Glu157Asp
NM_001384280.1:c.471G>C	NP_001371209.1:p.Glu157Asp
NM_001384290.1:c.456G>C MANE Select	NP_001371219.1:p.Glu152Asp
NM_002127.6:c.456G>C	NP_002118.1:p.Glu152Asp