Canonical Allele Identifier: CA2430395562
Gene: PAGE2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.55031140C= , CM000685.2:g.55031140C= GRCh38
NC_000023.10:g.55057573C= , CM000685.1:g.55057573C= GRCh37
NC_000023.9:g.55074298C= NCBI36
NG_008983.1:g.4925G=

Transcript Alleles

HGVS Amino-acid Change
XM_011530785.1:c.61+1468C= XP_011529087.1:n.61+1468C=
XM_011530786.1:c.7+165C= XP_011529088.1:n.7+165C=
XM_011530785.2:c.61+1468C= XP_011529087.1:n.61+1468C=
XM_011530786.3:c.7+165C= XP_011529088.1:n.7+165C=