Canonical Allele Identifier: CA421567620

Gene: RXRG

Linked Data

• MyVariant Identifiers: chr1:g.165389162G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419925G>T , CM000663.2:g.165419925G>T	GRCh38
NC_000001.10:g.165389162G>T , CM000663.1:g.165389162G>T	GRCh37
NC_000001.9:g.163655786G>T	NCBI36
NG_029517.1:g.30431C>A
NG_029517.2:g.30431C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.387C>A MANE Select	ENSP00000352900.5:p.Thr129=
ENST00000359842.9:c.387C>A	ENSP00000352900.5:p.Thr129=
ENST00000470566.1:n.312C>A
ENST00000619224.1:c.18C>A	ENSP00000482458.1:p.Thr6=
NM_001256570.1:c.18C>A	NP_001243499.1:p.Thr6=
NM_001256571.1:c.18C>A	NP_001243500.1:p.Thr6=
NM_006917.4:c.387C>A	NP_008848.1:p.Thr129=
NM_006917.5:c.387C>A MANE Select	NP_008848.1:p.Thr129=
NM_001256571.2:c.18C>A	NP_001243500.1:p.Thr6=
NM_001256570.2:c.18C>A	NP_001243499.1:p.Thr6=