Canonical Allele Identifier: CA1926063595
Gene: PAPSS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727522G= , CM000672.2:g.87727522G= GRCh38
NC_000010.10:g.89487279G= , CM000672.1:g.89487279G= GRCh37
NC_000010.9:g.89477259G= NCBI36
NG_012150.1:g.72804G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.1086+33G= MANE Select ENSP00000406157.1:n.1086+33G=
ENST00000361175.8:c.1071+33G= ENSP00000354436.4:n.1071+33G=
ENST00000456849.1:c.1086+33G= ENSP00000406157.1:n.1086+33G=
NM_001015880.1:c.1086+33G= NP_001015880.1:n.1086+33G=
NM_004670.3:c.1071+33G= NP_004661.2:n.1071+33G=
NM_001015880.2:c.1086+33G= MANE Select NP_001015880.1:n.1086+33G=
NM_004670.4:c.1071+33G= NP_004661.2:n.1071+33G=
Search 100 bp 5'
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