Canonical Allele Identifier: CA823759010

Gene: HLA-G

Linked Data

• dbSNP Id: rs1432962159
• gnomAD v4: 6-29830855-C-T
• MyVariant Identifiers: chr6:g.29798632C>T (hg19) ; chr6:g.29830855C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29830855C>T , CM000668.2:g.29830855C>T	GRCh38
NC_000006.11:g.29798632C>T , CM000668.1:g.29798632C>T	GRCh37
NC_000006.10:g.29906611C>T	NCBI36
NG_029039.1:g.8877C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360323.11:c.*116C>T MANE Select	ENSP00000353472.6:n.*116C>T
ENST00000360323.10:c.*116C>T	ENSP00000353472.6:n.*116C>T
ENST00000376815.3:c.581C>T	ENSP00000366011.3:n.581C>T
ENST00000376818.7:c.857C>T	ENSP00000366014.3:n.857C>T
ENST00000376828.6:c.*116C>T	ENSP00000366024.2:n.*116C>T
ENST00000428701.5:c.*116C>T	ENSP00000412927.1:n.*116C>T
ENST00000478355.5:n.1255C>T
ENST00000478519.5:c.905C>T	ENSP00000436375.1:n.905C>T
NM_002127.5:c.*116C>T	NP_002118.1:n.*116C>T
NM_001363567.1:c.*116C>T	NP_001350496.1:n.*116C>T
XM_017010817.1:c.*116C>T	XP_016866306.1:n.*116C>T
NM_001363567.2:c.*116C>T	NP_001350496.1:n.*116C>T
NM_001384280.1:c.*116C>T	NP_001371209.1:n.*116C>T
NM_001384290.1:c.*116C>T MANE Select	NP_001371219.1:n.*116C>T
NM_002127.6:c.*116C>T	NP_002118.1:n.*116C>T