Canonical Allele Identifier: CA2693865049
Gene: PAGE2B HGNC NCBI

Linked Data

gnomAD v4: X-55031196-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.55031196C>G , CM000685.2:g.55031196C>G GRCh38
NC_000023.10:g.55057629C>G , CM000685.1:g.55057629C>G GRCh37
NC_000023.9:g.55074354C>G NCBI36
NG_008983.1:g.4869G>C

Transcript Alleles

HGVS Amino-acid Change
XM_011530785.1:c.61+1524C>G XP_011529087.1:n.61+1524C>G
XM_011530786.1:c.7+221C>G XP_011529088.1:n.7+221C>G
XM_011530785.2:c.61+1524C>G XP_011529087.1:n.61+1524C>G
XM_011530786.3:c.7+221C>G XP_011529088.1:n.7+221C>G
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