Canonical Allele Identifier: CA421567594

Gene: RXRG

Linked Data

• MyVariant Identifiers: chr1:g.165389132A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419895A>G , CM000663.2:g.165419895A>G	GRCh38
NC_000001.10:g.165389132A>G , CM000663.1:g.165389132A>G	GRCh37
NC_000001.9:g.163655756A>G	NCBI36
NG_029517.1:g.30461T>C
NG_029517.2:g.30461T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000359842.10:c.417T>C MANE Select	ENSP00000352900.5:p.Cys139=
ENST00000359842.9:c.417T>C	ENSP00000352900.5:p.Cys139=
ENST00000470566.1:n.342T>C
ENST00000619224.1:c.48T>C	ENSP00000482458.1:p.Cys16=
NM_001256570.1:c.48T>C	NP_001243499.1:p.Cys16=
NM_001256571.1:c.48T>C	NP_001243500.1:p.Cys16=
NM_006917.4:c.417T>C	NP_008848.1:p.Cys139=
NM_006917.5:c.417T>C MANE Select	NP_008848.1:p.Cys139=
NM_001256571.2:c.48T>C	NP_001243500.1:p.Cys16=
NM_001256570.2:c.48T>C	NP_001243499.1:p.Cys16=