Canonical Allele Identifier: CA343472979

Gene: RXRG

Linked Data

• MyVariant Identifiers: chr1:g.165389196A>G (hg19) ; chr1:g.165419959A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419959A>G , CM000663.2:g.165419959A>G	GRCh38
NC_000001.10:g.165389196A>G , CM000663.1:g.165389196A>G	GRCh37
NC_000001.9:g.163655820A>G	NCBI36
NG_029517.1:g.30397T>C
NG_029517.2:g.30397T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.353T>C MANE Select	ENSP00000352900.5:p.Leu118Pro
ENST00000359842.9:c.353T>C	ENSP00000352900.5:p.Leu118Pro
ENST00000470566.1:n.278T>C
ENST00000619224.1:c.-17T>C	ENSP00000482458.1:n.-17T>C
NM_001256570.1:c.-17T>C	NP_001243499.1:n.-17T>C
NM_001256571.1:c.-17T>C	NP_001243500.1:n.-17T>C
NM_006917.4:c.353T>C	NP_008848.1:p.Leu118Pro
NM_006917.5:c.353T>C MANE Select	NP_008848.1:p.Leu118Pro
NM_001256571.2:c.-17T>C	NP_001243500.1:n.-17T>C
NM_001256570.2:c.-17T>C	NP_001243499.1:n.-17T>C