Canonical Allele Identifier: CA377485168
Gene: PAPSS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.89468969C>G (hg19) chr10:g.87709212C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87709212C>G , CM000672.2:g.87709212C>G GRCh38
NC_000010.10:g.89468969C>G , CM000672.1:g.89468969C>G GRCh37
NC_000010.9:g.89458949C>G NCBI36
NG_012150.1:g.54494C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000456849.2:c.44C>G MANE Select ENSP00000406157.1:p.Ser15Cys
ENST00000361175.8:c.44C>G ENSP00000354436.4:p.Ser15Cys
ENST00000456849.1:c.44C>G ENSP00000406157.1:p.Ser15Cys
ENST00000465996.5:n.66C>G
ENST00000482258.1:n.87C>G
NM_001015880.1:c.44C>G NP_001015880.1:p.Ser15Cys
NM_004670.3:c.44C>G NP_004661.2:p.Ser15Cys
NM_001015880.2:c.44C>G MANE Select NP_001015880.1:p.Ser15Cys
NM_004670.4:c.44C>G NP_004661.2:p.Ser15Cys
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