Canonical Allele Identifier: CA1619908116

Gene: RXRB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33198257A= , CM000668.2:g.33198257A=	GRCh38
NC_000006.11:g.33166034A= , CM000668.1:g.33166034A=	GRCh37
NC_000006.10:g.33274012A=	NCBI36
NG_023374.1:g.7399T=

Transcript Alleles

HGVS	Amino-acid Change
NM_021976.5:c.640+51T= MANE Select	NP_068811.1:n.640+51T=
ENST00000374680.4:c.640+51T= MANE Select	ENSP00000363812.3:n.640+51T=
NM_001270401.1:c.640+51T=	NP_001257330.1:n.640+51T=
NM_001270401.2:c.640+51T=	NP_001257330.1:n.640+51T=
NM_001291989.1:c.70+51T=	NP_001278918.1:n.70+51T=
NM_001291989.2:c.70+51T=	NP_001278918.1:n.70+51T=
NM_021976.4:c.640+51T=	NP_068811.1:n.640+51T=
ENST00000374680.3:c.640+51T=	ENSP00000363812.3:n.640+51T=
ENST00000374685.8:c.640+51T=	ENSP00000363817.4:n.640+51T=
ENST00000481441.1:n.328+51T=
ENST00000483281.5:c.*152+51T=	ENSP00000431369.1:n.*152+51T=
XM_005249278.1:c.352+51T=	XP_005249335.1:n.352+51T=
XM_005249278.3:c.352+51T=	XP_005249335.1:n.352+51T=
XM_005249279.1:c.352+51T=	XP_005249336.1:n.352+51T=
XM_011514796.1:c.289+51T=	XP_011513098.1:n.289+51T=
XM_011514796.3:c.289+51T=	XP_011513098.1:n.289+51T=
XM_017011176.1:c.271+51T=	XP_016866665.1:n.271+51T=
XR_926297.1:n.836+51T=