Canonical Allele Identifier: CA1926063598

Gene: PAPSS2

Linked Data

• dbSNP Id: rs1853675722
• gnomAD v4: 10-87727525-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87727525C>T , CM000672.2:g.87727525C>T	GRCh38
NC_000010.10:g.89487282C>T , CM000672.1:g.89487282C>T	GRCh37
NC_000010.9:g.89477262C>T	NCBI36
NG_012150.1:g.72807C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.1086+36C>T MANE Select	ENSP00000406157.1:n.1086+36C>T
ENST00000361175.8:c.1071+36C>T	ENSP00000354436.4:n.1071+36C>T
ENST00000456849.1:c.1086+36C>T	ENSP00000406157.1:n.1086+36C>T
NM_001015880.1:c.1086+36C>T	NP_001015880.1:n.1086+36C>T
NM_004670.3:c.1071+36C>T	NP_004661.2:n.1071+36C>T
NM_001015880.2:c.1086+36C>T MANE Select	NP_001015880.1:n.1086+36C>T
NM_004670.4:c.1071+36C>T	NP_004661.2:n.1071+36C>T