Canonical Allele Identifier: CA515946088
Gene: NR0B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.30326515G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308398G>C , CM000685.2:g.30308398G>C GRCh38
NC_000023.10:g.30326515G>C , CM000685.1:g.30326515G>C GRCh37
NC_000023.9:g.30236436G>C NCBI36
NG_009814.1:g.5981C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.966C>G MANE Select ENSP00000368253.4:p.Thr322=
ENST00000378963.1:c.81C>G ENSP00000368246.1:p.Thr27=
ENST00000378970.4:c.966C>G ENSP00000368253.4:p.Thr322=
NM_000475.4:c.966C>G NP_000466.2:p.Thr322=
NM_000475.5:c.966C>G MANE Select NP_000466.2:p.Thr322=
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Search 100 bp 3'