Canonical Allele Identifier: CA377489655
Gene: PAPSS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.89487223T>A (hg19) chr10:g.87727466T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727466T>A , CM000672.2:g.87727466T>A GRCh38
NC_000010.10:g.89487223T>A , CM000672.1:g.89487223T>A GRCh37
NC_000010.9:g.89477203T>A NCBI36
NG_012150.1:g.72748T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.1063T>A MANE Select ENSP00000406157.1:p.Cys355Ser
ENST00000361175.8:c.1048T>A ENSP00000354436.4:p.Cys350Ser
ENST00000456849.1:c.1063T>A ENSP00000406157.1:p.Cys355Ser
NM_001015880.1:c.1063T>A NP_001015880.1:p.Cys355Ser
NM_004670.3:c.1048T>A NP_004661.2:p.Cys350Ser
NM_001015880.2:c.1063T>A MANE Select NP_001015880.1:p.Cys355Ser
NM_004670.4:c.1048T>A NP_004661.2:p.Cys350Ser
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