Canonical Allele Identifier: CA3751827
Community Standard Title: NM_021976.5(RXRB):c.1373G>A (p.Ser458Asn)
Gene: RXRB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33195026C>T , CM000668.2:g.33195026C>T GRCh38
NC_000006.11:g.33162803C>T , CM000668.1:g.33162803C>T GRCh37
NC_000006.10:g.33270781C>T NCBI36
NG_011589.1:g.2443G>A
NG_023374.1:g.10630G>A

Transcript Alleles

HGVS Amino-acid Change
NM_021976.5:c.1373G>A MANE Select NP_068811.1:p.Ser458Asn
ENST00000374680.4:c.1373G>A MANE Select ENSP00000363812.3:p.Ser458Asn
NM_001270401.1:c.1385G>A NP_001257330.1:p.Ser462Asn
NM_001270401.2:c.1385G>A NP_001257330.1:p.Ser462Asn
NM_001291989.1:c.815G>A NP_001278918.1:p.Ser272Asn
NM_001291989.2:c.815G>A NP_001278918.1:p.Ser272Asn
NM_021976.4:c.1373G>A NP_068811.1:p.Ser458Asn
ENST00000374680.3:c.1373G>A ENSP00000363812.3:p.Ser458Asn
ENST00000374685.8:c.1385G>A ENSP00000363817.4:p.Ser462Asn
ENST00000483281.5:c.*885G>A ENSP00000431369.1:n.*885G>A
ENST00000483821.1:n.335G>A
XM_005249278.1:c.1097G>A XP_005249335.1:p.Ser366Asn
XM_005249278.3:c.1097G>A XP_005249335.1:p.Ser366Asn
XM_005249279.1:c.1085G>A XP_005249336.1:p.Ser362Asn
XM_011514796.1:c.1034G>A XP_011513098.1:p.Ser345Asn
XM_011514796.3:c.1034G>A XP_011513098.1:p.Ser345Asn
XM_017011176.1:c.1016G>A XP_016866665.1:p.Ser339Asn
XR_926297.1:n.1477G>A