Canonical Allele Identifier: CA2820256700

Gene: NR0B1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.30308145C>G , CM000685.2:g.30308145C>G	GRCh38
NC_000023.10:g.30326262C>G , CM000685.1:g.30326262C>G	GRCh37
NC_000023.9:g.30236183C>G	NCBI36
NG_009814.1:g.6234G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378970.5:c.1168+51G>C MANE Select	ENSP00000368253.4:n.1168+51G>C
ENST00000378963.1:c.283+51G>C	ENSP00000368246.1:n.283+51G>C
ENST00000378970.4:c.1168+51G>C	ENSP00000368253.4:n.1168+51G>C
NM_000475.4:c.1168+51G>C	NP_000466.2:n.1168+51G>C
NM_000475.5:c.1168+51G>C MANE Select	NP_000466.2:n.1168+51G>C