Canonical Allele Identifier: CA211255359

Gene: PAPSS2

Linked Data

• dbSNP Id: rs902579655
• MyVariant Identifiers: chr10:g.89468972C>G (hg19) ; chr10:g.87709215C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87709215C>G , CM000672.2:g.87709215C>G	GRCh38
NC_000010.10:g.89468972C>G , CM000672.1:g.89468972C>G	GRCh37
NC_000010.9:g.89458952C>G	NCBI36
NG_012150.1:g.54497C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000456849.2:c.47C>G MANE Select	ENSP00000406157.1:p.Thr16Ser
ENST00000361175.8:c.47C>G	ENSP00000354436.4:p.Thr16Ser
ENST00000456849.1:c.47C>G	ENSP00000406157.1:p.Thr16Ser
ENST00000465996.5:n.69C>G
ENST00000482258.1:n.90C>G
NM_001015880.1:c.47C>G	NP_001015880.1:p.Thr16Ser
NM_004670.3:c.47C>G	NP_004661.2:p.Thr16Ser
NM_001015880.2:c.47C>G MANE Select	NP_001015880.1:p.Thr16Ser
NM_004670.4:c.47C>G	NP_004661.2:p.Thr16Ser