Canonical Allele Identifier: CA1926063599
Gene: PAPSS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727528T= , CM000672.2:g.87727528T= GRCh38
NC_000010.10:g.89487285T= , CM000672.1:g.89487285T= GRCh37
NC_000010.9:g.89477265T= NCBI36
NG_012150.1:g.72810T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.1086+39T= MANE Select ENSP00000406157.1:n.1086+39T=
ENST00000361175.8:c.1071+39T= ENSP00000354436.4:n.1071+39T=
ENST00000456849.1:c.1086+39T= ENSP00000406157.1:n.1086+39T=
NM_001015880.1:c.1086+39T= NP_001015880.1:n.1086+39T=
NM_004670.3:c.1071+39T= NP_004661.2:n.1071+39T=
NM_001015880.2:c.1086+39T= MANE Select NP_001015880.1:n.1086+39T=
NM_004670.4:c.1071+39T= NP_004661.2:n.1071+39T=
Search 100 bp 5'
Search 100 bp 3'