Canonical Allele Identifier: CA377489321
Gene: PAPSS2 HGNC NCBI

Linked Data

dbSNP Id: rs1308403790

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727305T>C , CM000672.2:g.87727305T>C GRCh38
NC_000010.10:g.89487062T>C , CM000672.1:g.89487062T>C GRCh37
NC_000010.9:g.89477042T>C NCBI36
NG_012150.1:g.72587T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.902T>C MANE Select ENSP00000406157.1:p.Ile301Thr
ENST00000361175.8:c.887T>C ENSP00000354436.4:p.Ile296Thr
ENST00000456849.1:c.902T>C ENSP00000406157.1:p.Ile301Thr
NM_001015880.1:c.902T>C NP_001015880.1:p.Ile301Thr
NM_004670.3:c.887T>C NP_004661.2:p.Ile296Thr
NM_001015880.2:c.902T>C MANE Select NP_001015880.1:p.Ile301Thr
NM_004670.4:c.887T>C NP_004661.2:p.Ile296Thr