Canonical Allele Identifier: CA1926073351
Gene: PAPSS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87709348A= , CM000672.2:g.87709348A= GRCh38
NC_000010.10:g.89469105A= , CM000672.1:g.89469105A= GRCh37
NC_000010.9:g.89459085A= NCBI36
NG_012150.1:g.54630A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.145+35A= MANE Select ENSP00000406157.1:n.145+35A=
ENST00000361175.8:c.145+35A= ENSP00000354436.4:n.145+35A=
ENST00000456849.1:c.145+35A= ENSP00000406157.1:n.145+35A=
ENST00000465996.5:n.167+35A=
ENST00000482258.1:n.188+35A=
NM_001015880.1:c.145+35A= NP_001015880.1:n.145+35A=
NM_004670.3:c.145+35A= NP_004661.2:n.145+35A=
NM_001015880.2:c.145+35A= MANE Select NP_001015880.1:n.145+35A=
NM_004670.4:c.145+35A= NP_004661.2:n.145+35A=
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