Canonical Allele Identifier: CA2422040445

Gene: NR0B1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.30308420C= , CM000685.2:g.30308420C=	GRCh38
NC_000023.10:g.30326537C= , CM000685.1:g.30326537C=	GRCh37
NC_000023.9:g.30236458C=	NCBI36
NG_009814.1:g.5959G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378970.5:c.944G= MANE Select	ENSP00000368253.4:p.Ser315=
ENST00000378963.1:c.59G=	ENSP00000368246.1:p.Ser20=
ENST00000378970.4:c.944G=	ENSP00000368253.4:p.Ser315=
NM_000475.4:c.944G=	NP_000466.2:p.Ser315=
NM_000475.5:c.944G= MANE Select	NP_000466.2:p.Ser315=