Canonical Allele Identifier: CA412544271
Gene: NR0B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304587T>A , CM000685.2:g.30304587T>A GRCh38
NC_000023.10:g.30322704T>A , CM000685.1:g.30322704T>A GRCh37
NC_000023.9:g.30232625T>A NCBI36
NG_009814.1:g.9792A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378970.5:c.1405A>T MANE Select ENSP00000368253.4:p.Lys469Ter
ENST00000378970.4:c.1405A>T ENSP00000368253.4:p.Lys469Ter
NM_000475.4:c.1405A>T NP_000466.2:p.Lys469Ter
NM_000475.5:c.1405A>T MANE Select NP_000466.2:p.Lys469Ter