Canonical Allele Identifier: CA363046683

Gene: HLA-G

Linked Data

• dbSNP Id: rs1581664187
• gnomAD v3: 6-29828618-A-T
• gnomAD v4: 6-29828618-A-T
• MyVariant Identifiers: chr6:g.29796395A>T (hg19) ; chr6:g.29828618A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29828618A>T , CM000668.2:g.29828618A>T	GRCh38
NC_000006.11:g.29796395A>T , CM000668.1:g.29796395A>T	GRCh37
NC_000006.10:g.29904374A>T	NCBI36
NG_029039.1:g.6640A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000428701.6:n.523A>T
ENST00000360323.11:c.419A>T MANE Select	ENSP00000353472.6:p.Tyr140Phe
ENST00000360323.10:c.419A>T	ENSP00000353472.6:p.Tyr140Phe
ENST00000376815.3:c.343+302A>T	ENSP00000366011.3:n.343+302A>T
ENST00000376818.7:c.343+302A>T	ENSP00000366014.3:n.343+302A>T
ENST00000376828.6:c.434A>T	ENSP00000366024.2:p.Tyr145Phe
ENST00000428701.5:c.419A>T	ENSP00000412927.1:p.Tyr140Phe
ENST00000478355.5:n.419A>T
ENST00000478519.5:c.343+302A>T	ENSP00000436375.1:n.343+302A>T
NM_002127.5:c.419A>T	NP_002118.1:p.Tyr140Phe
NM_001363567.1:c.434A>T	NP_001350496.1:p.Tyr145Phe
XM_017010817.1:c.343+302A>T	XP_016866306.1:n.343+302A>T
XM_017010818.1:c.343+302A>T	XP_016866307.1:n.343+302A>T
XM_024446420.1:c.419A>T	XP_024302188.1:p.Tyr140Phe
NM_001363567.2:c.434A>T	NP_001350496.1:p.Tyr145Phe
NM_001384280.1:c.434A>T	NP_001371209.1:p.Tyr145Phe
NM_001384290.1:c.419A>T MANE Select	NP_001371219.1:p.Tyr140Phe
NM_002127.6:c.419A>T	NP_002118.1:p.Tyr140Phe