Canonical Allele Identifier: CA2422040298
Gene: NR0B1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308050T= , CM000685.2:g.30308050T= GRCh38
NC_000023.10:g.30326167T= , CM000685.1:g.30326167T= GRCh37
NC_000023.9:g.30236088T= NCBI36
NG_009814.1:g.6329A=

Transcript Alleles

HGVS Amino-acid change
ENST00000378970.5:c.1168+146A= MANE Select ENSP00000368253.4:n.1168+146A=
ENST00000378963.1:c.283+146A= ENSP00000368246.1:n.283+146A=
ENST00000378970.4:c.1168+146A= ENSP00000368253.4:n.1168+146A=
NM_000475.4:c.1168+146A= NP_000466.2:n.1168+146A=
NM_000475.5:c.1168+146A= MANE Select NP_000466.2:n.1168+146A=
Search 100 bp 5'
Search 100 bp 3'