Canonical Allele Identifier: CA3691798
Gene: HLA-G HGNC NCBI

Linked Data

dbSNP Id: rs76011433
gnomAD v2: 6-29796347-G-A
gnomAD v3: 6-29828570-G-A
gnomAD v4: 6-29828570-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29828570G>A , CM000668.2:g.29828570G>A GRCh38
NC_000006.11:g.29796347G>A , CM000668.1:g.29796347G>A GRCh37
NC_000006.10:g.29904326G>A NCBI36
NG_029039.1:g.6592G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000428701.6:n.522-47G>A
ENST00000360323.11:c.371G>A MANE Select ENSP00000353472.6:p.Gly124Asp
ENST00000360323.10:c.371G>A ENSP00000353472.6:p.Gly124Asp
ENST00000376815.3:c.343+254G>A ENSP00000366011.3:n.343+254G>A
ENST00000376818.7:c.343+254G>A ENSP00000366014.3:n.343+254G>A
ENST00000376828.6:c.386G>A ENSP00000366024.2:p.Gly129Asp
ENST00000428701.5:c.371G>A ENSP00000412927.1:p.Gly124Asp
ENST00000478355.5:n.371G>A
ENST00000478519.5:c.343+254G>A ENSP00000436375.1:n.343+254G>A
NM_002127.5:c.371G>A NP_002118.1:p.Gly124Asp
NM_001363567.1:c.386G>A NP_001350496.1:p.Gly129Asp
XM_017010817.1:c.343+254G>A XP_016866306.1:n.343+254G>A
XM_017010818.1:c.343+254G>A XP_016866307.1:n.343+254G>A
XM_024446420.1:c.371G>A XP_024302188.1:p.Gly124Asp
NM_001363567.2:c.386G>A NP_001350496.1:p.Gly129Asp
NM_001384280.1:c.386G>A NP_001371209.1:p.Gly129Asp
NM_001384290.1:c.371G>A MANE Select NP_001371219.1:p.Gly124Asp
NM_002127.6:c.371G>A NP_002118.1:p.Gly124Asp