Canonical Allele Identifier: CA2430395584
Gene: PAGE2B HGNC NCBI

Linked Data

dbSNP Id: rs1935996089
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.55031183A>G , CM000685.2:g.55031183A>G GRCh38
NC_000023.10:g.55057616A>G , CM000685.1:g.55057616A>G GRCh37
NC_000023.9:g.55074341A>G NCBI36
NG_008983.1:g.4882T>C

Transcript Alleles

HGVS Amino-acid Change
XM_011530785.1:c.61+1511A>G XP_011529087.1:n.61+1511A>G
XM_011530786.1:c.7+208A>G XP_011529088.1:n.7+208A>G
XM_011530785.2:c.61+1511A>G XP_011529087.1:n.61+1511A>G
XM_011530786.3:c.7+208A>G XP_011529088.1:n.7+208A>G
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