Canonical Allele Identifier: CA343472980

Gene: RXRG

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.353T>A MANE Select	ENSP00000352900.5:p.Leu118His
ENST00000359842.9:c.353T>A	ENSP00000352900.5:p.Leu118His
ENST00000470566.1:n.278T>A
ENST00000619224.1:c.-17T>A	ENSP00000482458.1:n.-17T>A
NM_001256570.1:c.-17T>A	NP_001243499.1:n.-17T>A
NM_001256571.1:c.-17T>A	NP_001243500.1:n.-17T>A
NM_006917.4:c.353T>A	NP_008848.1:p.Leu118His
NM_006917.5:c.353T>A MANE Select	NP_008848.1:p.Leu118His
NM_001256571.2:c.-17T>A	NP_001243500.1:n.-17T>A
NM_001256570.2:c.-17T>A	NP_001243499.1:n.-17T>A