Canonical Allele Identifier: CA2740089232

Gene: RXRG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419711G>T , CM000663.2:g.165419711G>T	GRCh38
NC_000001.10:g.165388948G>T , CM000663.1:g.165388948G>T	GRCh37
NC_000001.9:g.163655572G>T	NCBI36
NG_029517.1:g.30645C>A
NG_029517.2:g.30645C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.442+159C>A MANE Select	ENSP00000352900.5:n.442+159C>A
ENST00000359842.9:c.442+159C>A	ENSP00000352900.5:n.442+159C>A
ENST00000470566.1:n.367+159C>A
ENST00000619224.1:c.73+159C>A	ENSP00000482458.1:n.73+159C>A
NM_001256570.1:c.73+159C>A	NP_001243499.1:n.73+159C>A
NM_001256571.1:c.73+159C>A	NP_001243500.1:n.73+159C>A
NM_006917.4:c.442+159C>A	NP_008848.1:n.442+159C>A
NM_006917.5:c.442+159C>A MANE Select	NP_008848.1:n.442+159C>A
NM_001256571.2:c.73+159C>A	NP_001243500.1:n.73+159C>A
NM_001256570.2:c.73+159C>A	NP_001243499.1:n.73+159C>A