Canonical Allele Identifier: CA658114120
Gene: PAGE2B HGNC NCBI

Linked Data

gnomAD v4: X-55031193-G-A
COSMIC: COSN19275265
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.55031193G>A , CM000685.2:g.55031193G>A GRCh38
NC_000023.10:g.55057626G>A , CM000685.1:g.55057626G>A GRCh37
NC_000023.9:g.55074351G>A NCBI36
NG_008983.1:g.4872C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011530785.1:c.61+1521G>A XP_011529087.1:n.61+1521G>A
XM_011530786.1:c.7+218G>A XP_011529088.1:n.7+218G>A
XM_011530785.2:c.61+1521G>A XP_011529087.1:n.61+1521G>A
XM_011530786.3:c.7+218G>A XP_011529088.1:n.7+218G>A
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