Canonical Allele Identifier: CA10376301
Gene: NR0B1 HGNC NCBI

Linked Data

dbSNP Id: rs372326021
ExAC: X:30326262 C / T
gnomAD v2: X-30326262-C-T
gnomAD v3: X-30308145-C-T
gnomAD v4: X-30308145-C-T
MyVariant Identifiers: chrX:g.30326262C>T (hg19) chrX:g.30308145C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308145C>T , CM000685.2:g.30308145C>T GRCh38
NC_000023.10:g.30326262C>T , CM000685.1:g.30326262C>T GRCh37
NC_000023.9:g.30236183C>T NCBI36
NG_009814.1:g.6234G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378970.5:c.1168+51G>A MANE Select ENSP00000368253.4:n.1168+51G>A
ENST00000378963.1:c.283+51G>A ENSP00000368246.1:n.283+51G>A
ENST00000378970.4:c.1168+51G>A ENSP00000368253.4:n.1168+51G>A
NM_000475.4:c.1168+51G>A NP_000466.2:n.1168+51G>A
NM_000475.5:c.1168+51G>A MANE Select NP_000466.2:n.1168+51G>A
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