Canonical Allele Identifier: CA470668752
Gene: PAPSS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.89487168T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727411T>A , CM000672.2:g.87727411T>A GRCh38
NC_000010.10:g.89487168T>A , CM000672.1:g.89487168T>A GRCh37
NC_000010.9:g.89477148T>A NCBI36
NG_012150.1:g.72693T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.1008T>A MANE Select ENSP00000406157.1:p.Ala336=
ENST00000361175.8:c.993T>A ENSP00000354436.4:p.Ala331=
ENST00000456849.1:c.1008T>A ENSP00000406157.1:p.Ala336=
NM_001015880.1:c.1008T>A NP_001015880.1:p.Ala336=
NM_004670.3:c.993T>A NP_004661.2:p.Ala331=
NM_001015880.2:c.1008T>A MANE Select NP_001015880.1:p.Ala336=
NM_004670.4:c.993T>A NP_004661.2:p.Ala331=
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Search 100 bp 3'