Canonical Allele Identifier: CA15448111
Gene: HLA-G HGNC NCBI

Linked Data

dbSNP Id: rs9380142
gnomAD v2: 6-29798794-A-G
gnomAD v3: 6-29831017-A-G
gnomAD v4: 6-29831017-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29831017A>G , CM000668.2:g.29831017A>G GRCh38
NC_000006.11:g.29798794A>G , CM000668.1:g.29798794A>G GRCh37
NC_000006.10:g.29906773A>G NCBI36
NG_029039.1:g.9039A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360323.11:c.*278A>G MANE Select ENSP00000353472.6:n.*278A>G
ENST00000360323.10:c.*278A>G ENSP00000353472.6:n.*278A>G
ENST00000376815.3:c.743A>G ENSP00000366011.3:n.743A>G
ENST00000376818.7:c.1019A>G ENSP00000366014.3:n.1019A>G
ENST00000376828.6:c.*278A>G ENSP00000366024.2:n.*278A>G
ENST00000428701.5:c.*278A>G ENSP00000412927.1:n.*278A>G
ENST00000478355.5:n.1417A>G
ENST00000478519.5:c.1067A>G ENSP00000436375.1:n.1067A>G
NM_002127.5:c.*278A>G NP_002118.1:n.*278A>G
NM_001363567.1:c.*278A>G NP_001350496.1:n.*278A>G
XM_017010817.1:c.*278A>G XP_016866306.1:n.*278A>G
NM_001363567.2:c.*278A>G NP_001350496.1:n.*278A>G
NM_001384280.1:c.*278A>G NP_001371209.1:n.*278A>G
NM_001384290.1:c.*278A>G MANE Select NP_001371219.1:n.*278A>G
NM_002127.6:c.*278A>G NP_002118.1:n.*278A>G