Canonical Allele Identifier: CA377489546
Gene: PAPSS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.89487173T>A (hg19) chr10:g.87727416T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727416T>A , CM000672.2:g.87727416T>A GRCh38
NC_000010.10:g.89487173T>A , CM000672.1:g.89487173T>A GRCh37
NC_000010.9:g.89477153T>A NCBI36
NG_012150.1:g.72698T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.1013T>A MANE Select ENSP00000406157.1:p.Phe338Tyr
ENST00000361175.8:c.998T>A ENSP00000354436.4:p.Phe333Tyr
ENST00000456849.1:c.1013T>A ENSP00000406157.1:p.Phe338Tyr
NM_001015880.1:c.1013T>A NP_001015880.1:p.Phe338Tyr
NM_004670.3:c.998T>A NP_004661.2:p.Phe333Tyr
NM_001015880.2:c.1013T>A MANE Select NP_001015880.1:p.Phe338Tyr
NM_004670.4:c.998T>A NP_004661.2:p.Phe333Tyr
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