Canonical Allele Identifier: CA2677781966

Gene: HLA-G

Linked Data

• gnomAD v4: 6-29831032-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29831032C>T , CM000668.2:g.29831032C>T	GRCh38
NC_000006.11:g.29798809C>T , CM000668.1:g.29798809C>T	GRCh37
NC_000006.10:g.29906788C>T	NCBI36
NG_029039.1:g.9054C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360323.10:c.*293C>T	ENSP00000353472.6:n.*293C>T
ENST00000376815.3:c.758C>T	ENSP00000366011.3:n.758C>T
ENST00000376818.7:c.1034C>T	ENSP00000366014.3:n.1034C>T
ENST00000376828.6:c.*293C>T	ENSP00000366024.2:n.*293C>T
ENST00000428701.5:c.*293C>T	ENSP00000412927.1:n.*293C>T
ENST00000478355.5:n.1432C>T
ENST00000478519.5:c.1082C>T	ENSP00000436375.1:n.1082C>T
NM_002127.5:c.*293C>T	NP_002118.1:n.*293C>T
NM_001363567.1:c.*293C>T	NP_001350496.1:n.*293C>T
XM_017010817.1:c.*293C>T	XP_016866306.1:n.*293C>T