Canonical Allele Identifier: CA412544457
Gene: NR0B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304666A>T , CM000685.2:g.30304666A>T GRCh38
NC_000023.10:g.30322783A>T , CM000685.1:g.30322783A>T GRCh37
NC_000023.9:g.30232704A>T NCBI36
NG_009814.1:g.9713T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.1326T>A MANE Select ENSP00000368253.4:p.Asn442Lys
ENST00000378970.4:c.1326T>A ENSP00000368253.4:p.Asn442Lys
NM_000475.4:c.1326T>A NP_000466.2:p.Asn442Lys
NM_000475.5:c.1326T>A MANE Select NP_000466.2:p.Asn442Lys