Canonical Allele Identifier: CA2842699510
Gene: NR0B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304567G>T , CM000685.2:g.30304567G>T GRCh38
NC_000023.10:g.30322684G>T , CM000685.1:g.30322684G>T GRCh37
NC_000023.9:g.30232605G>T NCBI36
NG_009814.1:g.9812C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.*12C>A MANE Select ENSP00000368253.4:n.*12C>A
ENST00000378970.4:c.*12C>A ENSP00000368253.4:n.*12C>A
NM_000475.4:c.*12C>A NP_000466.2:n.*12C>A
NM_000475.5:c.*12C>A MANE Select NP_000466.2:n.*12C>A
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