Canonical Allele Identifier: CA2579577171
Gene: NR0B1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30304512T>C , CM000685.2:g.30304512T>C GRCh38
NC_000023.10:g.30322629T>C , CM000685.1:g.30322629T>C GRCh37
NC_000023.9:g.30232550T>C NCBI36
NG_009814.1:g.9867A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.*67A>G MANE Select ENSP00000368253.4:n.*67A>G
ENST00000378970.4:c.*67A>G ENSP00000368253.4:n.*67A>G
NM_000475.4:c.*67A>G NP_000466.2:n.*67A>G
NM_000475.5:c.*67A>G MANE Select NP_000466.2:n.*67A>G
Search 100 bp 5'
Search 100 bp 3'