Canonical Allele Identifier: CA470663094

Gene: PAPSS2

Linked Data

• MyVariant Identifiers: chr10:g.89469039T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87709282T>G , CM000672.2:g.87709282T>G	GRCh38
NC_000010.10:g.89469039T>G , CM000672.1:g.89469039T>G	GRCh37
NC_000010.9:g.89459019T>G	NCBI36
NG_012150.1:g.54564T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.114T>G MANE Select	ENSP00000406157.1:p.Gly38=
ENST00000361175.8:c.114T>G	ENSP00000354436.4:p.Gly38=
ENST00000456849.1:c.114T>G	ENSP00000406157.1:p.Gly38=
ENST00000465996.5:n.136T>G
ENST00000482258.1:n.157T>G
NM_001015880.1:c.114T>G	NP_001015880.1:p.Gly38=
NM_004670.3:c.114T>G	NP_004661.2:p.Gly38=
NM_001015880.2:c.114T>G MANE Select	NP_001015880.1:p.Gly38=
NM_004670.4:c.114T>G	NP_004661.2:p.Gly38=