Canonical Allele Identifier: CA2693382700
Gene: NR0B1 HGNC NCBI

Linked Data

gnomAD v4: X-30304484-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304484G>T , CM000685.2:g.30304484G>T GRCh38
NC_000023.10:g.30322601G>T , CM000685.1:g.30322601G>T GRCh37
NC_000023.9:g.30232522G>T NCBI36
NG_009814.1:g.9895C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.*95C>A MANE Select ENSP00000368253.4:n.*95C>A
ENST00000378970.4:c.*95C>A ENSP00000368253.4:n.*95C>A
NM_000475.4:c.*95C>A NP_000466.2:n.*95C>A
NM_000475.5:c.*95C>A MANE Select NP_000466.2:n.*95C>A
Search 100 bp 5'
Search 100 bp 3'