Canonical Allele Identifier: CA2677781676

Gene: HLA-G

Linked Data

• gnomAD v4: 6-29830849-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29830849C>G , CM000668.2:g.29830849C>G	GRCh38
NC_000006.11:g.29798626C>G , CM000668.1:g.29798626C>G	GRCh37
NC_000006.10:g.29906605C>G	NCBI36
NG_029039.1:g.8871C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360323.11:c.*110C>G MANE Select	ENSP00000353472.6:n.*110C>G
ENST00000360323.10:c.*110C>G	ENSP00000353472.6:n.*110C>G
ENST00000376815.3:c.575C>G	ENSP00000366011.3:n.575C>G
ENST00000376818.7:c.851C>G	ENSP00000366014.3:n.851C>G
ENST00000376828.6:c.*110C>G	ENSP00000366024.2:n.*110C>G
ENST00000428701.5:c.*110C>G	ENSP00000412927.1:n.*110C>G
ENST00000478355.5:n.1249C>G
ENST00000478519.5:c.899C>G	ENSP00000436375.1:n.899C>G
NM_002127.5:c.*110C>G	NP_002118.1:n.*110C>G
NM_001363567.1:c.*110C>G	NP_001350496.1:n.*110C>G
XM_017010817.1:c.*110C>G	XP_016866306.1:n.*110C>G
NM_001363567.2:c.*110C>G	NP_001350496.1:n.*110C>G
NM_001384280.1:c.*110C>G	NP_001371209.1:n.*110C>G
NM_001384290.1:c.*110C>G MANE Select	NP_001371219.1:n.*110C>G
NM_002127.6:c.*110C>G	NP_002118.1:n.*110C>G