Canonical Allele Identifier: CA339188463

Gene: NR0B2 NUDC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26912036C>G , CM000663.2:g.26912036C>G	GRCh38
NC_000001.10:g.27238527C>G , CM000663.1:g.27238527C>G	GRCh37
NC_000001.9:g.27111114C>G	NCBI36
NG_012143.1:g.7041G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_021969.3:c.583G>C (NR0B2) MANE Select	NP_068804.1:p.Ala195Pro
ENST00000254227.4:c.583G>C (NR0B2) MANE Select	ENSP00000254227.3:p.Ala195Pro
NM_021969.2:c.583G>C (NR0B2)	NP_068804.1:p.Ala195Pro
ENST00000254227.3:c.583G>C (NR0B2)	ENSP00000254227.3:p.Ala195Pro
ENST00000435827.6:c.93+801C>G (NUDC)	ENSP00000404020.2:n.93+801C>G
XM_011540529.1:c.93+801C>G (NUDC)	XP_011538831.1:n.93+801C>G
XM_017000094.1:c.93+801C>G (NUDC)	XP_016855583.1:n.93+801C>G
XM_024452486.1:c.93+801C>G (NUDC)	XP_024308254.1:n.93+801C>G