Canonical Allele Identifier: CA470662893
Gene: PAPSS2 HGNC NCBI

Linked Data

gnomAD v4: 10-87709213-C-A
MyVariant Identifiers: chr10:g.89468970C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87709213C>A , CM000672.2:g.87709213C>A GRCh38
NC_000010.10:g.89468970C>A , CM000672.1:g.89468970C>A GRCh37
NC_000010.9:g.89458950C>A NCBI36
NG_012150.1:g.54495C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000456849.2:c.45C>A MANE Select ENSP00000406157.1:p.Ser15=
ENST00000361175.8:c.45C>A ENSP00000354436.4:p.Ser15=
ENST00000456849.1:c.45C>A ENSP00000406157.1:p.Ser15=
ENST00000465996.5:n.67C>A
ENST00000482258.1:n.88C>A
NM_001015880.1:c.45C>A NP_001015880.1:p.Ser15=
NM_004670.3:c.45C>A NP_004661.2:p.Ser15=
NM_001015880.2:c.45C>A MANE Select NP_001015880.1:p.Ser15=
NM_004670.4:c.45C>A NP_004661.2:p.Ser15=
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