Canonical Allele Identifier: CA2422040479
Gene: NR0B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308516T= , CM000685.2:g.30308516T= GRCh38
NC_000023.10:g.30326633T= , CM000685.1:g.30326633T= GRCh37
NC_000023.9:g.30236554T= NCBI36
NG_009814.1:g.5863A=

Transcript Alleles

HGVS Amino-acid change
ENST00000378970.5:c.848A= MANE Select ENSP00000368253.4:p.Gln283=
ENST00000378970.4:c.848A= ENSP00000368253.4:p.Gln283=
NM_000475.4:c.848A= NP_000466.2:p.Gln283=
NM_000475.5:c.848A= MANE Select NP_000466.2:p.Gln283=