Canonical Allele Identifier: CA1140073996

Gene: NR0B2 NUDC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26913429C= , CM000663.2:g.26913429C=	GRCh38
NC_000001.10:g.27239920C= , CM000663.1:g.27239920C=	GRCh37
NC_000001.9:g.27112507C=	NCBI36
NG_012143.1:g.5648G=

Transcript Alleles

HGVS	Amino-acid Change
NM_021969.3:c.512G= (NR0B2) MANE Select	NP_068804.1:p.Gly171=
ENST00000254227.4:c.512G= (NR0B2) MANE Select	ENSP00000254227.3:p.Gly171=
NM_021969.2:c.512G= (NR0B2)	NP_068804.1:p.Gly171=
ENST00000254227.3:c.512G= (NR0B2)	ENSP00000254227.3:p.Gly171=
ENST00000435827.6:c.93+2194C= (NUDC)	ENSP00000404020.2:n.93+2194C=
XM_011540529.1:c.93+2194C= (NUDC)	XP_011538831.1:n.93+2194C=
XM_011542297.1:c.512G= (NR0B2)	XP_011540599.1:p.Gly171=
XM_011542297.3:c.512G= (NR0B2)	XP_011540599.1:p.Gly171=
XM_017000094.1:c.93+2194C= (NUDC)	XP_016855583.1:n.93+2194C=
XM_024452486.1:c.93+2194C= (NUDC)	XP_024308254.1:n.93+2194C=