Canonical Allele Identifier: CA329227002
Gene: PAGE3 HGNC NCBI

Linked Data

dbSNP Id: rs4240023
gnomAD v2: X-55393079-T-C
gnomAD v3: X-55366646-T-C
gnomAD v4: X-55366646-T-C
MyVariant Identifiers: chrX:g.55393079T>C (hg19) chrX:g.55366646T>C (hg38)
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Genomic Alleles

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

Transcript Alleles

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