Canonical Allele Identifier: CA2693382712
Gene: NR0B1 HGNC NCBI

Linked Data

gnomAD v4: X-30304513-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304516del , CM000685.2:g.30304516del GRCh38
NC_000023.10:g.30322633del , CM000685.1:g.30322633del GRCh37
NC_000023.9:g.30232554del NCBI36
NG_009814.1:g.9865del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.*65del MANE Select ENSP00000368253.4:n.*65del
ENST00000378970.4:c.*65del ENSP00000368253.4:n.*65del
NM_000475.4:c.*65del NP_000466.2:n.*65del
NM_000475.5:c.*65del MANE Select NP_000466.2:n.*65del
Search 100 bp 5'
Search 100 bp 3'