Canonical Allele Identifier: CA377485170

Gene: PAPSS2

Linked Data

• MyVariant Identifiers: chr10:g.89468971A>T (hg19) ; chr10:g.87709214A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87709214A>T , CM000672.2:g.87709214A>T	GRCh38
NC_000010.10:g.89468971A>T , CM000672.1:g.89468971A>T	GRCh37
NC_000010.9:g.89458951A>T	NCBI36
NG_012150.1:g.54496A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000456849.2:c.46A>T MANE Select	ENSP00000406157.1:p.Thr16Ser
ENST00000361175.8:c.46A>T	ENSP00000354436.4:p.Thr16Ser
ENST00000456849.1:c.46A>T	ENSP00000406157.1:p.Thr16Ser
ENST00000465996.5:n.68A>T
ENST00000482258.1:n.89A>T
NM_001015880.1:c.46A>T	NP_001015880.1:p.Thr16Ser
NM_004670.3:c.46A>T	NP_004661.2:p.Thr16Ser
NM_001015880.2:c.46A>T MANE Select	NP_001015880.1:p.Thr16Ser
NM_004670.4:c.46A>T	NP_004661.2:p.Thr16Ser