Canonical Allele Identifier: CA343472826

Gene: RXRG

Linked Data

• MyVariant Identifiers: chr1:g.165389124C>G (hg19) ; chr1:g.165419887C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419887C>G , CM000663.2:g.165419887C>G	GRCh38
NC_000001.10:g.165389124C>G , CM000663.1:g.165389124C>G	GRCh37
NC_000001.9:g.163655748C>G	NCBI36
NG_029517.1:g.30469G>C
NG_029517.2:g.30469G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.425G>C MANE Select	ENSP00000352900.5:p.Cys142Ser
ENST00000359842.9:c.425G>C	ENSP00000352900.5:p.Cys142Ser
ENST00000470566.1:n.350G>C
ENST00000619224.1:c.56G>C	ENSP00000482458.1:p.Cys19Ser
NM_001256570.1:c.56G>C	NP_001243499.1:p.Cys19Ser
NM_001256571.1:c.56G>C	NP_001243500.1:p.Cys19Ser
NM_006917.4:c.425G>C	NP_008848.1:p.Cys142Ser
NM_006917.5:c.425G>C MANE Select	NP_008848.1:p.Cys142Ser
NM_001256571.2:c.56G>C	NP_001243500.1:p.Cys19Ser
NM_001256570.2:c.56G>C	NP_001243499.1:p.Cys19Ser