Canonical Allele Identifier: CA876477189
Gene: PAGE3 HGNC NCBI

Linked Data

dbSNP Id: rs1317624152
MyVariant Identifiers: chrX:g.55393022A>G (hg19) chrX:g.55366589A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.55366589A>G , CM000685.2:g.55366589A>G GRCh38
NC_000023.10:g.55393022A>G , CM000685.1:g.55393022A>G GRCh37
NC_000023.9:g.55409747A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011530765.1:c.-9+95055T>C XP_011529067.1:n.-9+95055T>C
XM_011530766.1:c.-9+95055T>C XP_011529068.1:n.-9+95055T>C
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