Canonical Allele Identifier: CA1204419931

Gene: RXRG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165440032C= , CM000663.2:g.165440032C=	GRCh38
NC_000001.10:g.165409269C= , CM000663.1:g.165409269C=	GRCh37
NC_000001.9:g.163675893C=	NCBI36
NG_029517.1:g.10324G=
NG_029517.2:g.10324G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359842.10:c.49+4813G= MANE Select	ENSP00000352900.5:n.49+4813G=
ENST00000359842.9:c.49+4813G=	ENSP00000352900.5:n.49+4813G=
ENST00000465764.1:n.329-2831G=
ENST00000619224.1:c.-379+4813G=	ENSP00000482458.1:n.-379+4813G=
NM_001256570.1:c.-379+4813G=	NP_001243499.1:n.-379+4813G=
NM_006917.4:c.49+4813G=	NP_008848.1:n.49+4813G=
NR_033824.1:n.512-2831G=
NM_006917.5:c.49+4813G= MANE Select	NP_008848.1:n.49+4813G=
NR_033824.2:n.283-2831G=
NM_001256570.2:c.-379+4813G=	NP_001243499.1:n.-379+4813G=