Canonical Allele Identifier: CA2693382726
Gene: NR0B1 HGNC NCBI

Linked Data

gnomAD v4: X-30304554-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304554C>T , CM000685.2:g.30304554C>T GRCh38
NC_000023.10:g.30322671C>T , CM000685.1:g.30322671C>T GRCh37
NC_000023.9:g.30232592C>T NCBI36
NG_009814.1:g.9825G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.*25G>A MANE Select ENSP00000368253.4:n.*25G>A
ENST00000378970.4:c.*25G>A ENSP00000368253.4:n.*25G>A
NM_000475.4:c.*25G>A NP_000466.2:n.*25G>A
NM_000475.5:c.*25G>A MANE Select NP_000466.2:n.*25G>A
Search 100 bp 5'
Search 100 bp 3'