Canonical Allele Identifier: CA343473027

Gene: RXRG

Linked Data

• dbSNP Id: rs1658258176
• MyVariant Identifiers: chr1:g.165389219C>G (hg19) ; chr1:g.165419982C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419982C>G , CM000663.2:g.165419982C>G	GRCh38
NC_000001.10:g.165389219C>G , CM000663.1:g.165389219C>G	GRCh37
NC_000001.9:g.163655843C>G	NCBI36
NG_029517.1:g.30374G>C
NG_029517.2:g.30374G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.330G>C MANE Select	ENSP00000352900.5:p.Glu110Asp
ENST00000359842.9:c.330G>C	ENSP00000352900.5:p.Glu110Asp
ENST00000470566.1:n.255G>C
ENST00000619224.1:c.-40G>C	ENSP00000482458.1:n.-40G>C
NM_001256570.1:c.-40G>C	NP_001243499.1:n.-40G>C
NM_001256571.1:c.-40G>C	NP_001243500.1:n.-40G>C
NM_006917.4:c.330G>C	NP_008848.1:p.Glu110Asp
NM_006917.5:c.330G>C MANE Select	NP_008848.1:p.Glu110Asp
NM_001256571.2:c.-40G>C	NP_001243500.1:n.-40G>C
NM_001256570.2:c.-40G>C	NP_001243499.1:n.-40G>C