Canonical Allele Identifier: CA2820261570
Gene: NR0B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304538A>C , CM000685.2:g.30304538A>C GRCh38
NC_000023.10:g.30322655A>C , CM000685.1:g.30322655A>C GRCh37
NC_000023.9:g.30232576A>C NCBI36
NG_009814.1:g.9841T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.*41T>G MANE Select ENSP00000368253.4:n.*41T>G
ENST00000378970.4:c.*41T>G ENSP00000368253.4:n.*41T>G
NM_000475.4:c.*41T>G NP_000466.2:n.*41T>G
NM_000475.5:c.*41T>G MANE Select NP_000466.2:n.*41T>G