Canonical Allele Identifier: CA343472938

Gene: RXRG

Linked Data

• MyVariant Identifiers: chr1:g.165389177C>T (hg19) ; chr1:g.165419940C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419940C>T , CM000663.2:g.165419940C>T	GRCh38
NC_000001.10:g.165389177C>T , CM000663.1:g.165389177C>T	GRCh37
NC_000001.9:g.163655801C>T	NCBI36
NG_029517.1:g.30416G>A
NG_029517.2:g.30416G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.372G>A MANE Select	ENSP00000352900.5:p.Met124Ile
ENST00000359842.9:c.372G>A	ENSP00000352900.5:p.Met124Ile
ENST00000470566.1:n.297G>A
ENST00000619224.1:c.3G>A	ENSP00000482458.1:p.Met1Ile
NM_001256570.1:c.3G>A	NP_001243499.1:p.Met1Ile
NM_001256571.1:c.3G>A	NP_001243500.1:p.Met1Ile
NM_006917.4:c.372G>A	NP_008848.1:p.Met124Ile
NM_006917.5:c.372G>A MANE Select	NP_008848.1:p.Met124Ile
NM_001256571.2:c.3G>A	NP_001243500.1:p.Met1Ile
NM_001256570.2:c.3G>A	NP_001243499.1:p.Met1Ile