Canonical Allele Identifier: CA5589601
Gene: PAPSS2 HGNC NCBI

Linked Data

dbSNP Id: rs368206390

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727287G>A , CM000672.2:g.87727287G>A GRCh38
NC_000010.10:g.89487044G>A , CM000672.1:g.89487044G>A GRCh37
NC_000010.9:g.89477024G>A NCBI36
NG_012150.1:g.72569G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.884G>A MANE Select ENSP00000406157.1:p.Gly295Asp
ENST00000361175.8:c.869G>A ENSP00000354436.4:p.Gly290Asp
ENST00000456849.1:c.884G>A ENSP00000406157.1:p.Gly295Asp
NM_001015880.1:c.884G>A NP_001015880.1:p.Gly295Asp
NM_004670.3:c.869G>A NP_004661.2:p.Gly290Asp
NM_001015880.2:c.884G>A MANE Select NP_001015880.1:p.Gly295Asp
NM_004670.4:c.869G>A NP_004661.2:p.Gly290Asp