Canonical Allele Identifier: CA412548121
Gene: NR0B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.30326808C>A (hg19) chrX:g.30308691C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308691C>A , CM000685.2:g.30308691C>A GRCh38
NC_000023.10:g.30326808C>A , CM000685.1:g.30326808C>A GRCh37
NC_000023.9:g.30236729C>A NCBI36
NG_009814.1:g.5688G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.673G>T MANE Select ENSP00000368253.4:p.Ala225Ser
ENST00000378970.4:c.673G>T ENSP00000368253.4:p.Ala225Ser
NM_000475.4:c.673G>T NP_000466.2:p.Ala225Ser
NM_000475.5:c.673G>T MANE Select NP_000466.2:p.Ala225Ser
Search 100 bp 5'
Search 100 bp 3'