Canonical Allele Identifier: CA515946034
Gene: NR0B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.30326497G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308380G>T , CM000685.2:g.30308380G>T GRCh38
NC_000023.10:g.30326497G>T , CM000685.1:g.30326497G>T GRCh37
NC_000023.9:g.30236418G>T NCBI36
NG_009814.1:g.5999C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.984C>A MANE Select ENSP00000368253.4:p.Thr328=
ENST00000378963.1:c.99C>A ENSP00000368246.1:p.Thr33=
ENST00000378970.4:c.984C>A ENSP00000368253.4:p.Thr328=
NM_000475.4:c.984C>A NP_000466.2:p.Thr328=
NM_000475.5:c.984C>A MANE Select NP_000466.2:p.Thr328=
Search 100 bp 5'
Search 100 bp 3'