Canonical Allele Identifier: CA470662980

Gene: PAPSS2

Linked Data

• dbSNP Id: rs2131931553
• gnomAD v4: 10-87709231-G-A
• MyVariant Identifiers: chr10:g.89468988G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87709231G>A , CM000672.2:g.87709231G>A	GRCh38
NC_000010.10:g.89468988G>A , CM000672.1:g.89468988G>A	GRCh37
NC_000010.9:g.89458968G>A	NCBI36
NG_012150.1:g.54513G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.63G>A MANE Select	ENSP00000406157.1:p.Gln21=
ENST00000361175.8:c.63G>A	ENSP00000354436.4:p.Gln21=
ENST00000456849.1:c.63G>A	ENSP00000406157.1:p.Gln21=
ENST00000465996.5:n.85G>A
ENST00000482258.1:n.106G>A
NM_001015880.1:c.63G>A	NP_001015880.1:p.Gln21=
NM_004670.3:c.63G>A	NP_004661.2:p.Gln21=
NM_001015880.2:c.63G>A MANE Select	NP_001015880.1:p.Gln21=
NM_004670.4:c.63G>A	NP_004661.2:p.Gln21=