Canonical Allele Identifier: CA2842699496
Gene: NR0B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304496dup , CM000685.2:g.30304496dup GRCh38
NC_000023.10:g.30322613dup , CM000685.1:g.30322613dup GRCh37
NC_000023.9:g.30232534dup NCBI36
NG_009814.1:g.9886dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.*86dup MANE Select ENSP00000368253.4:n.*86dup
ENST00000378970.4:c.*86dup ENSP00000368253.4:n.*86dup
NM_000475.4:c.*86dup NP_000466.2:n.*86dup
NM_000475.5:c.*86dup MANE Select NP_000466.2:n.*86dup
Search 100 bp 5'
Search 100 bp 3'