Canonical Allele Identifier: CA1618466786

Gene: HLA-G

Linked Data

• dbSNP Id: rs1761239689

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29831044_29831045del , CM000668.2:g.29831044_29831045del	GRCh38
NC_000006.11:g.29798821_29798822del , CM000668.1:g.29798821_29798822del	GRCh37
NC_000006.10:g.29906800_29906801del	NCBI36
NG_029039.1:g.9066_9067del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360323.10:c.*305_*306del	ENSP00000353472.6:n.*305_*306del
ENST00000376815.3:c.770_771del	ENSP00000366011.3:n.770_771del
ENST00000376818.7:c.1046_1047del	ENSP00000366014.3:n.1046_1047del
ENST00000376828.6:c.*305_*306del	ENSP00000366024.2:n.*305_*306del
ENST00000428701.5:c.*305_*306del	ENSP00000412927.1:n.*305_*306del
ENST00000478355.5:n.1444_1445del
ENST00000478519.5:c.1094_1095del	ENSP00000436375.1:n.1094_1095del
NM_002127.5:c.*305_*306del	NP_002118.1:n.*305_*306del
NM_001363567.1:c.*305_*306del	NP_001350496.1:n.*305_*306del
XM_017010817.1:c.*305_*306del	XP_016866306.1:n.*305_*306del