Canonical Allele Identifier: CA1204410049

Gene: RXRG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165419700T= , CM000663.2:g.165419700T=	GRCh38
NC_000001.10:g.165388937T= , CM000663.1:g.165388937T=	GRCh37
NC_000001.9:g.163655561T=	NCBI36
NG_029517.1:g.30656A=
NG_029517.2:g.30656A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.442+170A= MANE Select	ENSP00000352900.5:n.442+170A=
ENST00000359842.9:c.442+170A=	ENSP00000352900.5:n.442+170A=
ENST00000470566.1:n.367+170A=
ENST00000619224.1:c.73+170A=	ENSP00000482458.1:n.73+170A=
NM_001256570.1:c.73+170A=	NP_001243499.1:n.73+170A=
NM_001256571.1:c.73+170A=	NP_001243500.1:n.73+170A=
NM_006917.4:c.442+170A=	NP_008848.1:n.442+170A=
NM_006917.5:c.442+170A= MANE Select	NP_008848.1:n.442+170A=
NM_001256571.2:c.73+170A=	NP_001243500.1:n.73+170A=
NM_001256570.2:c.73+170A=	NP_001243499.1:n.73+170A=