Canonical Allele Identifier: CA328978798

Gene: PAGE2B

Linked Data

• dbSNP Id: rs1052014840
• gnomAD v3: X-55031237-T-A
• gnomAD v4: X-55031237-T-A
• MyVariant Identifiers: chrX:g.55057670T>A (hg19) ; chrX:g.55031237T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.55031237T>A , CM000685.2:g.55031237T>A	GRCh38
NC_000023.10:g.55057670T>A , CM000685.1:g.55057670T>A	GRCh37
NC_000023.9:g.55074395T>A	NCBI36
NG_008983.1:g.4828A>T

Transcript Alleles

HGVS	Amino-acid Change
XM_011530785.1:c.61+1565T>A	XP_011529087.1:n.61+1565T>A
XM_011530786.1:c.7+262T>A	XP_011529088.1:n.7+262T>A
XM_011530785.2:c.61+1565T>A	XP_011529087.1:n.61+1565T>A
XM_011530786.3:c.7+262T>A	XP_011529088.1:n.7+262T>A