Canonical Allele Identifier: CA412546693
Gene: NR0B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308304A>T , CM000685.2:g.30308304A>T GRCh38
NC_000023.10:g.30326421A>T , CM000685.1:g.30326421A>T GRCh37
NC_000023.9:g.30236342A>T NCBI36
NG_009814.1:g.6075T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.1060T>A MANE Select ENSP00000368253.4:p.Ser354Thr
ENST00000378963.1:c.175T>A ENSP00000368246.1:p.Ser59Thr
ENST00000378970.4:c.1060T>A ENSP00000368253.4:p.Ser354Thr
NM_000475.4:c.1060T>A NP_000466.2:p.Ser354Thr
NM_000475.5:c.1060T>A MANE Select NP_000466.2:p.Ser354Thr