Canonical Allele Identifier: CA876477198
Gene: PAGE3 HGNC NCBI

Linked Data

dbSNP Id: rs4240023
MyVariant Identifiers: chrX:g.55393079T>A (hg19) chrX:g.55366646T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.55366646T>A , CM000685.2:g.55366646T>A GRCh38
NC_000023.10:g.55393079T>A , CM000685.1:g.55393079T>A GRCh37
NC_000023.9:g.55409804T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011530765.1:c.-9+94998A>T XP_011529067.1:n.-9+94998A>T
XM_011530766.1:c.-9+94998A>T XP_011529068.1:n.-9+94998A>T
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