Canonical Allele Identifier: CA2422040450
Gene: NR0B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308428C= , CM000685.2:g.30308428C= GRCh38
NC_000023.10:g.30326545C= , CM000685.1:g.30326545C= GRCh37
NC_000023.9:g.30236466C= NCBI36
NG_009814.1:g.5951G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378970.5:c.936G= MANE Select ENSP00000368253.4:p.Ser312=
ENST00000378963.1:c.51G= ENSP00000368246.1:p.Ser17=
ENST00000378970.4:c.936G= ENSP00000368253.4:p.Ser312=
NM_000475.4:c.936G= NP_000466.2:p.Ser312=
NM_000475.5:c.936G= MANE Select NP_000466.2:p.Ser312=