Canonical Allele Identifier: CA515945876
Gene: NR0B1 HGNC NCBI

Linked Data

dbSNP Id: rs1926563298
MyVariant Identifiers: chrX:g.30326431C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308314C>T , CM000685.2:g.30308314C>T GRCh38
NC_000023.10:g.30326431C>T , CM000685.1:g.30326431C>T GRCh37
NC_000023.9:g.30236352C>T NCBI36
NG_009814.1:g.6065G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.1050G>A MANE Select ENSP00000368253.4:p.Arg350=
ENST00000378963.1:c.165G>A ENSP00000368246.1:p.Arg55=
ENST00000378970.4:c.1050G>A ENSP00000368253.4:p.Arg350=
NM_000475.4:c.1050G>A NP_000466.2:p.Arg350=
NM_000475.5:c.1050G>A MANE Select NP_000466.2:p.Arg350=
Search 100 bp 5'
Search 100 bp 3'