Canonical Allele Identifier: CA1132010663
Gene: NR0B1 HGNC NCBI

Linked Data

dbSNP Id: rs2070828768
gnomAD v3: X-30304568-C-T
gnomAD v4: X-30304568-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304568C>T , CM000685.2:g.30304568C>T GRCh38
NC_000023.10:g.30322685C>T , CM000685.1:g.30322685C>T GRCh37
NC_000023.9:g.30232606C>T NCBI36
NG_009814.1:g.9811G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.*11G>A MANE Select ENSP00000368253.4:n.*11G>A
ENST00000378970.4:c.*11G>A ENSP00000368253.4:n.*11G>A
NM_000475.4:c.*11G>A NP_000466.2:n.*11G>A
NM_000475.5:c.*11G>A MANE Select NP_000466.2:n.*11G>A
Search 100 bp 5'
Search 100 bp 3'