Canonical Allele Identifier: CA377485268

Gene: PAPSS2

Linked Data

• MyVariant Identifiers: chr10:g.89469015A>C (hg19) ; chr10:g.87709258A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87709258A>C , CM000672.2:g.87709258A>C	GRCh38
NC_000010.10:g.89469015A>C , CM000672.1:g.89469015A>C	GRCh37
NC_000010.9:g.89458995A>C	NCBI36
NG_012150.1:g.54540A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.90A>C MANE Select	ENSP00000406157.1:p.Arg30Ser
ENST00000361175.8:c.90A>C	ENSP00000354436.4:p.Arg30Ser
ENST00000456849.1:c.90A>C	ENSP00000406157.1:p.Arg30Ser
ENST00000465996.5:n.112A>C
ENST00000482258.1:n.133A>C
NM_001015880.1:c.90A>C	NP_001015880.1:p.Arg30Ser
NM_004670.3:c.90A>C	NP_004661.2:p.Arg30Ser
NM_001015880.2:c.90A>C MANE Select	NP_001015880.1:p.Arg30Ser
NM_004670.4:c.90A>C	NP_004661.2:p.Arg30Ser