Canonical Allele Identifier: CA2422040342
Gene: NR0B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308143C= , CM000685.2:g.30308143C= GRCh38
NC_000023.10:g.30326260C= , CM000685.1:g.30326260C= GRCh37
NC_000023.9:g.30236181C= NCBI36
NG_009814.1:g.6236G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378970.5:c.1168+53G= MANE Select ENSP00000368253.4:n.1168+53G=
ENST00000378963.1:c.283+53G= ENSP00000368246.1:n.283+53G=
ENST00000378970.4:c.1168+53G= ENSP00000368253.4:n.1168+53G=
NM_000475.4:c.1168+53G= NP_000466.2:n.1168+53G=
NM_000475.5:c.1168+53G= MANE Select NP_000466.2:n.1168+53G=