Canonical Allele Identifier: CA470668239

Gene: PAPSS2

Linked Data

• MyVariant Identifiers: chr10:g.89487111G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87727354G>T , CM000672.2:g.87727354G>T	GRCh38
NC_000010.10:g.89487111G>T , CM000672.1:g.89487111G>T	GRCh37
NC_000010.9:g.89477091G>T	NCBI36
NG_012150.1:g.72636G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.951G>T MANE Select	ENSP00000406157.1:p.Gly317=
ENST00000361175.8:c.936G>T	ENSP00000354436.4:p.Gly312=
ENST00000456849.1:c.951G>T	ENSP00000406157.1:p.Gly317=
NM_001015880.1:c.951G>T	NP_001015880.1:p.Gly317=
NM_004670.3:c.936G>T	NP_004661.2:p.Gly312=
NM_001015880.2:c.951G>T MANE Select	NP_001015880.1:p.Gly317=
NM_004670.4:c.936G>T	NP_004661.2:p.Gly312=