Canonical Allele Identifier: CA2693382697
Gene: NR0B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304473del , CM000685.2:g.30304473del GRCh38
NC_000023.10:g.30322590del , CM000685.1:g.30322590del GRCh37
NC_000023.9:g.30232511del NCBI36
NG_009814.1:g.9910del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.*110del MANE Select ENSP00000368253.4:n.*110del
ENST00000378970.4:c.*110del ENSP00000368253.4:n.*110del
NM_000475.4:c.*110del NP_000466.2:n.*110del
NM_000475.5:c.*110del MANE Select NP_000466.2:n.*110del