Canonical Allele Identifier: CA343472887

Gene: RXRG

Linked Data

• MyVariant Identifiers: chr1:g.165389152A>T (hg19) ; chr1:g.165419915A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419915A>T , CM000663.2:g.165419915A>T	GRCh38
NC_000001.10:g.165389152A>T , CM000663.1:g.165389152A>T	GRCh37
NC_000001.9:g.163655776A>T	NCBI36
NG_029517.1:g.30441T>A
NG_029517.2:g.30441T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.397T>A MANE Select	ENSP00000352900.5:p.Ser133Thr
ENST00000359842.9:c.397T>A	ENSP00000352900.5:p.Ser133Thr
ENST00000470566.1:n.322T>A
ENST00000619224.1:c.28T>A	ENSP00000482458.1:p.Ser10Thr
NM_001256570.1:c.28T>A	NP_001243499.1:p.Ser10Thr
NM_001256571.1:c.28T>A	NP_001243500.1:p.Ser10Thr
NM_006917.4:c.397T>A	NP_008848.1:p.Ser133Thr
NM_006917.5:c.397T>A MANE Select	NP_008848.1:p.Ser133Thr
NM_001256571.2:c.28T>A	NP_001243500.1:p.Ser10Thr
NM_001256570.2:c.28T>A	NP_001243499.1:p.Ser10Thr