Canonical Allele Identifier: CA470668102

Gene: PAPSS2

Linked Data

• MyVariant Identifiers: chr10:g.89487072A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87727315A>G , CM000672.2:g.87727315A>G	GRCh38
NC_000010.10:g.89487072A>G , CM000672.1:g.89487072A>G	GRCh37
NC_000010.9:g.89477052A>G	NCBI36
NG_012150.1:g.72597A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.912A>G MANE Select	ENSP00000406157.1:p.Val304=
ENST00000361175.8:c.897A>G	ENSP00000354436.4:p.Val299=
ENST00000456849.1:c.912A>G	ENSP00000406157.1:p.Val304=
NM_001015880.1:c.912A>G	NP_001015880.1:p.Val304=
NM_004670.3:c.897A>G	NP_004661.2:p.Val299=
NM_001015880.2:c.912A>G MANE Select	NP_001015880.1:p.Val304=
NM_004670.4:c.897A>G	NP_004661.2:p.Val299=