Canonical Allele Identifier: CA377489283
Gene: PAPSS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727290T>A , CM000672.2:g.87727290T>A GRCh38
NC_000010.10:g.89487047T>A , CM000672.1:g.89487047T>A GRCh37
NC_000010.9:g.89477027T>A NCBI36
NG_012150.1:g.72572T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.887T>A MANE Select ENSP00000406157.1:p.Val296Glu
ENST00000361175.8:c.872T>A ENSP00000354436.4:p.Val291Glu
ENST00000456849.1:c.887T>A ENSP00000406157.1:p.Val296Glu
NM_001015880.1:c.887T>A NP_001015880.1:p.Val296Glu
NM_004670.3:c.872T>A NP_004661.2:p.Val291Glu
NM_001015880.2:c.887T>A MANE Select NP_001015880.1:p.Val296Glu
NM_004670.4:c.872T>A NP_004661.2:p.Val291Glu