Canonical Allele Identifier: CA641383506
Gene: PAGE2B HGNC NCBI

Linked Data

dbSNP Id: rs1260882313
gnomAD v2: X-55057651-C-T
gnomAD v3: X-55031218-C-T
gnomAD v4: X-55031218-C-T
MyVariant Identifiers: chrX:g.55057651C>T (hg19) chrX:g.55031218C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.55031218C>T , CM000685.2:g.55031218C>T GRCh38
NC_000023.10:g.55057651C>T , CM000685.1:g.55057651C>T GRCh37
NC_000023.9:g.55074376C>T NCBI36
NG_008983.1:g.4847G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011530785.1:c.61+1546C>T XP_011529087.1:n.61+1546C>T
XM_011530786.1:c.7+243C>T XP_011529088.1:n.7+243C>T
XM_011530785.2:c.61+1546C>T XP_011529087.1:n.61+1546C>T
XM_011530786.3:c.7+243C>T XP_011529088.1:n.7+243C>T
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