Canonical Allele Identifier: CA1220195
Gene: RXRG HGNC NCBI

Linked Data

dbSNP Id: rs1128977

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165419892G>A , CM000663.2:g.165419892G>A GRCh38
NC_000001.10:g.165389129G>A , CM000663.1:g.165389129G>A GRCh37
NC_000001.9:g.163655753G>A NCBI36
NG_029517.1:g.30464C>T
NG_029517.2:g.30464C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000359842.10:c.420C>T MANE Select ENSP00000352900.5:p.Ala140=
ENST00000359842.9:c.420C>T ENSP00000352900.5:p.Ala140=
ENST00000470566.1:n.345C>T
ENST00000619224.1:c.51C>T ENSP00000482458.1:p.Ala17=
NM_001256570.1:c.51C>T NP_001243499.1:p.Ala17=
NM_001256571.1:c.51C>T NP_001243500.1:p.Ala17=
NM_006917.4:c.420C>T NP_008848.1:p.Ala140=
NM_006917.5:c.420C>T MANE Select NP_008848.1:p.Ala140=
NM_001256571.2:c.51C>T NP_001243500.1:p.Ala17=
NM_001256570.2:c.51C>T NP_001243499.1:p.Ala17=