Canonical Allele Identifier: CA2430395578

Gene: PAGE2B

Linked Data

• dbSNP Id: rs1935995762

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.55031175T>C , CM000685.2:g.55031175T>C	GRCh38
NC_000023.10:g.55057608T>C , CM000685.1:g.55057608T>C	GRCh37
NC_000023.9:g.55074333T>C	NCBI36
NG_008983.1:g.4890A>G

Transcript Alleles

HGVS	Amino-acid Change
XM_011530785.1:c.61+1503T>C	XP_011529087.1:n.61+1503T>C
XM_011530786.1:c.7+200T>C	XP_011529088.1:n.7+200T>C
XM_011530785.2:c.61+1503T>C	XP_011529087.1:n.61+1503T>C
XM_011530786.3:c.7+200T>C	XP_011529088.1:n.7+200T>C