Canonical Allele Identifier: CA470669209

Gene: PAPSS2

Linked Data

• MyVariant Identifiers: chr10:g.89487246A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87727489A>G , CM000672.2:g.87727489A>G	GRCh38
NC_000010.10:g.89487246A>G , CM000672.1:g.89487246A>G	GRCh37
NC_000010.9:g.89477226A>G	NCBI36
NG_012150.1:g.72771A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.1086A>G MANE Select	ENSP00000406157.1:p.Lys362=
ENST00000361175.8:c.1071A>G	ENSP00000354436.4:p.Lys357=
ENST00000456849.1:c.1086A>G	ENSP00000406157.1:p.Lys362=
NM_001015880.1:c.1086A>G	NP_001015880.1:p.Lys362=
NM_004670.3:c.1071A>G	NP_004661.2:p.Lys357=
NM_001015880.2:c.1086A>G MANE Select	NP_001015880.1:p.Lys362=
NM_004670.4:c.1071A>G	NP_004661.2:p.Lys357=