Canonical Allele Identifier: CA2422040482

Gene: NR0B1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.30308520G= , CM000685.2:g.30308520G=	GRCh38
NC_000023.10:g.30326637G= , CM000685.1:g.30326637G=	GRCh37
NC_000023.9:g.30236558G=	NCBI36
NG_009814.1:g.5859C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378970.5:c.844C= MANE Select	ENSP00000368253.4:p.Gln282=
ENST00000378970.4:c.844C=	ENSP00000368253.4:p.Gln282=
NM_000475.4:c.844C=	NP_000466.2:p.Gln282=
NM_000475.5:c.844C= MANE Select	NP_000466.2:p.Gln282=