Canonical Allele Identifier: CA2422039203
Gene: NR0B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304713T= , CM000685.2:g.30304713T= GRCh38
NC_000023.10:g.30322830T= , CM000685.1:g.30322830T= GRCh37
NC_000023.9:g.30232751T= NCBI36
NG_009814.1:g.9666A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.1279A= MANE Select ENSP00000368253.4:p.Ile427=
ENST00000378970.4:c.1279A= ENSP00000368253.4:p.Ile427=
NM_000475.4:c.1279A= NP_000466.2:p.Ile427=
NM_000475.5:c.1279A= MANE Select NP_000466.2:p.Ile427=