Canonical Allele Identifier: CA2422040449
Gene: NR0B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308427C= , CM000685.2:g.30308427C= GRCh38
NC_000023.10:g.30326544C= , CM000685.1:g.30326544C= GRCh37
NC_000023.9:g.30236465C= NCBI36
NG_009814.1:g.5952G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378970.5:c.937G= MANE Select ENSP00000368253.4:p.Glu313=
ENST00000378963.1:c.52G= ENSP00000368246.1:p.Glu18=
ENST00000378970.4:c.937G= ENSP00000368253.4:p.Glu313=
NM_000475.4:c.937G= NP_000466.2:p.Glu313=
NM_000475.5:c.937G= MANE Select NP_000466.2:p.Glu313=