Canonical Allele Identifier: CA377489499
Gene: PAPSS2 HGNC NCBI

Linked Data

gnomAD v4: 10-87727394-G-A
MyVariant Identifiers: chr10:g.89487151G>A (hg19) chr10:g.87727394G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727394G>A , CM000672.2:g.87727394G>A GRCh38
NC_000010.10:g.89487151G>A , CM000672.1:g.89487151G>A GRCh37
NC_000010.9:g.89477131G>A NCBI36
NG_012150.1:g.72676G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.991G>A MANE Select ENSP00000406157.1:p.Ala331Thr
ENST00000361175.8:c.976G>A ENSP00000354436.4:p.Ala326Thr
ENST00000456849.1:c.991G>A ENSP00000406157.1:p.Ala331Thr
NM_001015880.1:c.991G>A NP_001015880.1:p.Ala331Thr
NM_004670.3:c.976G>A NP_004661.2:p.Ala326Thr
NM_001015880.2:c.991G>A MANE Select NP_001015880.1:p.Ala331Thr
NM_004670.4:c.976G>A NP_004661.2:p.Ala326Thr
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