Canonical Allele Identifier: CA2422040527
Gene: NR0B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308679C= , CM000685.2:g.30308679C= GRCh38
NC_000023.10:g.30326796C= , CM000685.1:g.30326796C= GRCh37
NC_000023.9:g.30236717C= NCBI36
NG_009814.1:g.5700G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.685G= MANE Select ENSP00000368253.4:p.Glu229=
ENST00000378970.4:c.685G= ENSP00000368253.4:p.Glu229=
NM_000475.4:c.685G= NP_000466.2:p.Glu229=
NM_000475.5:c.685G= MANE Select NP_000466.2:p.Glu229=