Canonical Allele Identifier: CA2581570789

Gene: RXRB

Genomic Alleles

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

Transcript Alleles

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