Canonical Allele Identifier: CA377485180
Gene: PAPSS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.89468978T>A (hg19) chr10:g.87709221T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87709221T>A , CM000672.2:g.87709221T>A GRCh38
NC_000010.10:g.89468978T>A , CM000672.1:g.89468978T>A GRCh37
NC_000010.9:g.89458958T>A NCBI36
NG_012150.1:g.54503T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000456849.2:c.53T>A MANE Select ENSP00000406157.1:p.Val18Glu
ENST00000361175.8:c.53T>A ENSP00000354436.4:p.Val18Glu
ENST00000456849.1:c.53T>A ENSP00000406157.1:p.Val18Glu
ENST00000465996.5:n.75T>A
ENST00000482258.1:n.96T>A
NM_001015880.1:c.53T>A NP_001015880.1:p.Val18Glu
NM_004670.3:c.53T>A NP_004661.2:p.Val18Glu
NM_001015880.2:c.53T>A MANE Select NP_001015880.1:p.Val18Glu
NM_004670.4:c.53T>A NP_004661.2:p.Val18Glu
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