Canonical Allele Identifier: CA2842699506
Gene: NR0B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304560T>C , CM000685.2:g.30304560T>C GRCh38
NC_000023.10:g.30322677T>C , CM000685.1:g.30322677T>C GRCh37
NC_000023.9:g.30232598T>C NCBI36
NG_009814.1:g.9819A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.*19A>G MANE Select ENSP00000368253.4:n.*19A>G
ENST00000378970.4:c.*19A>G ENSP00000368253.4:n.*19A>G
NM_000475.4:c.*19A>G NP_000466.2:n.*19A>G
NM_000475.5:c.*19A>G MANE Select NP_000466.2:n.*19A>G
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