Canonical Allele Identifier: CA2677781666

Gene: HLA-G

Linked Data

• gnomAD v4: 6-29830845-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29830845G>C , CM000668.2:g.29830845G>C	GRCh38
NC_000006.11:g.29798622G>C , CM000668.1:g.29798622G>C	GRCh37
NC_000006.10:g.29906601G>C	NCBI36
NG_029039.1:g.8867G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360323.11:c.*106G>C MANE Select	ENSP00000353472.6:n.*106G>C
ENST00000360323.10:c.*106G>C	ENSP00000353472.6:n.*106G>C
ENST00000376815.3:c.571G>C	ENSP00000366011.3:n.571G>C
ENST00000376818.7:c.847G>C	ENSP00000366014.3:n.847G>C
ENST00000376828.6:c.*106G>C	ENSP00000366024.2:n.*106G>C
ENST00000428701.5:c.*106G>C	ENSP00000412927.1:n.*106G>C
ENST00000478355.5:n.1245G>C
ENST00000478519.5:c.895G>C	ENSP00000436375.1:n.895G>C
NM_002127.5:c.*106G>C	NP_002118.1:n.*106G>C
NM_001363567.1:c.*106G>C	NP_001350496.1:n.*106G>C
XM_017010817.1:c.*106G>C	XP_016866306.1:n.*106G>C
NM_001363567.2:c.*106G>C	NP_001350496.1:n.*106G>C
NM_001384280.1:c.*106G>C	NP_001371209.1:n.*106G>C
NM_001384290.1:c.*106G>C MANE Select	NP_001371219.1:n.*106G>C
NM_002127.6:c.*106G>C	NP_002118.1:n.*106G>C