Canonical Allele Identifier: CA412545398
Gene: NR0B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304749T>G , CM000685.2:g.30304749T>G GRCh38
NC_000023.10:g.30322866T>G , CM000685.1:g.30322866T>G GRCh37
NC_000023.9:g.30232787T>G NCBI36
NG_009814.1:g.9630A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.1243A>C MANE Select ENSP00000368253.4:p.Thr415Pro
ENST00000378970.4:c.1243A>C ENSP00000368253.4:p.Thr415Pro
NM_000475.4:c.1243A>C NP_000466.2:p.Thr415Pro
NM_000475.5:c.1243A>C MANE Select NP_000466.2:p.Thr415Pro