Canonical Allele Identifier: CA890586565

Gene: RXRG

Linked Data

• dbSNP Id: rs1235465408
• MyVariant Identifiers: chr1:g.165389293A>G (hg19) ; chr1:g.165420056A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165420056A>G , CM000663.2:g.165420056A>G	GRCh38
NC_000001.10:g.165389293A>G , CM000663.1:g.165389293A>G	GRCh37
NC_000001.9:g.163655917A>G	NCBI36
NG_029517.1:g.30300T>C
NG_029517.2:g.30300T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.298-42T>C MANE Select	ENSP00000352900.5:n.298-42T>C
ENST00000359842.9:c.298-42T>C	ENSP00000352900.5:n.298-42T>C
ENST00000470566.1:n.223-42T>C
ENST00000619224.1:c.-72-42T>C	ENSP00000482458.1:n.-72-42T>C
NM_001256570.1:c.-72-42T>C	NP_001243499.1:n.-72-42T>C
NM_001256571.1:c.-72-42T>C	NP_001243500.1:n.-72-42T>C
NM_006917.4:c.298-42T>C	NP_008848.1:n.298-42T>C
NM_006917.5:c.298-42T>C MANE Select	NP_008848.1:n.298-42T>C
NM_001256571.2:c.-72-42T>C	NP_001243500.1:n.-72-42T>C
NM_001256570.2:c.-72-42T>C	NP_001243499.1:n.-72-42T>C