Canonical Allele Identifier: CA363624255

Gene: RXRB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33198386C>T , CM000668.2:g.33198386C>T	GRCh38
NC_000006.11:g.33166163C>T , CM000668.1:g.33166163C>T	GRCh37
NC_000006.10:g.33274141C>T	NCBI36
NG_023374.1:g.7270G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374680.4:c.562G>A MANE Select	ENSP00000363812.3:p.Gly188Ser
ENST00000374680.3:c.562G>A	ENSP00000363812.3:p.Gly188Ser
ENST00000374685.8:c.562G>A	ENSP00000363817.4:p.Gly188Ser
ENST00000481441.1:n.250G>A
ENST00000483281.5:c.*74G>A	ENSP00000431369.1:n.*74G>A
NM_001270401.1:c.562G>A	NP_001257330.1:p.Gly188Ser
NM_001291989.1:c.17-25G>A	NP_001278918.1:n.17-25G>A
NM_021976.4:c.562G>A	NP_068811.1:p.Gly188Ser
XM_005249278.1:c.274G>A	XP_005249335.1:p.Gly92Ser
XM_005249279.1:c.274G>A	XP_005249336.1:p.Gly92Ser
XM_011514796.1:c.236-25G>A	XP_011513098.1:n.236-25G>A
XR_926297.1:n.758G>A
XM_005249278.3:c.274G>A	XP_005249335.1:p.Gly92Ser
XM_011514796.3:c.236-25G>A	XP_011513098.1:n.236-25G>A
XM_017011176.1:c.193G>A	XP_016866665.1:p.Gly65Ser
NM_001270401.2:c.562G>A	NP_001257330.1:p.Gly188Ser
NM_021976.5:c.562G>A MANE Select	NP_068811.1:p.Gly188Ser
NM_001291989.2:c.17-25G>A	NP_001278918.1:n.17-25G>A