Canonical Allele Identifier: CA10603722
Gene: NR0B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 279854
ClinVar RCV Id: RCV000260370
dbSNP Id: rs886041215

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304694del , CM000685.2:g.30304694del GRCh38
NC_000023.10:g.30322811del , CM000685.1:g.30322811del GRCh37
NC_000023.9:g.30232732del NCBI36
NG_009814.1:g.9688del

Transcript Alleles

HGVS Amino-acid change
ENST00000378970.5:c.1301del MANE Select ENSP00000368253.4:p.Phe434SerfsTer3
ENST00000378970.4:c.1301del ENSP00000368253.4:p.Phe434SerfsTer3
NM_000475.4:c.1301del NP_000466.2:p.Phe434SerfsTer3
NM_000475.5:c.1301del MANE Select NP_000466.2:p.Phe434SerfsTer3