Canonical Allele Identifier: CA2422039190
Gene: NR0B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304676A= , CM000685.2:g.30304676A= GRCh38
NC_000023.10:g.30322793A= , CM000685.1:g.30322793A= GRCh37
NC_000023.9:g.30232714A= NCBI36
NG_009814.1:g.9703T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.1316T= MANE Select ENSP00000368253.4:p.Ile439=
ENST00000378970.4:c.1316T= ENSP00000368253.4:p.Ile439=
NM_000475.4:c.1316T= NP_000466.2:p.Ile439=
NM_000475.5:c.1316T= MANE Select NP_000466.2:p.Ile439=
Search 100 bp 5'
Search 100 bp 3'