Canonical Allele Identifier: CA327976050
Gene: NR0B1 HGNC NCBI

Linked Data

dbSNP Id: rs898550666
gnomAD v2: X-30326759-C-A
gnomAD v4: X-30308642-C-A
MyVariant Identifiers: chrX:g.30326759C>A (hg19) chrX:g.30308642C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308642C>A , CM000685.2:g.30308642C>A GRCh38
NC_000023.10:g.30326759C>A , CM000685.1:g.30326759C>A GRCh37
NC_000023.9:g.30236680C>A NCBI36
NG_009814.1:g.5737G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.722G>T MANE Select ENSP00000368253.4:p.Gly241Val
ENST00000378970.4:c.722G>T ENSP00000368253.4:p.Gly241Val
NM_000475.4:c.722G>T NP_000466.2:p.Gly241Val
NM_000475.5:c.722G>T MANE Select NP_000466.2:p.Gly241Val
Search 100 bp 5'
Search 100 bp 3'