Canonical Allele Identifier: CA2422039232
Gene: NR0B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304798C= , CM000685.2:g.30304798C= GRCh38
NC_000023.10:g.30322915C= , CM000685.1:g.30322915C= GRCh37
NC_000023.9:g.30232836C= NCBI36
NG_009814.1:g.9581G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378970.5:c.1194G= MANE Select ENSP00000368253.4:p.Lys398=
ENST00000378970.4:c.1194G= ENSP00000368253.4:p.Lys398=
NM_000475.4:c.1194G= NP_000466.2:p.Lys398=
NM_000475.5:c.1194G= MANE Select NP_000466.2:p.Lys398=