Canonical Allele Identifier: CA2840294953
Gene: PAPSS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87709172G>T , CM000672.2:g.87709172G>T GRCh38
NC_000010.10:g.89468929G>T , CM000672.1:g.89468929G>T GRCh37
NC_000010.9:g.89458909G>T NCBI36
NG_012150.1:g.54454G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.28-24G>T MANE Select ENSP00000406157.1:n.28-24G>T
ENST00000361175.8:c.28-24G>T ENSP00000354436.4:n.28-24G>T
ENST00000456849.1:c.28-24G>T ENSP00000406157.1:n.28-24G>T
ENST00000465996.5:n.50-24G>T
ENST00000482258.1:n.71-24G>T
NM_001015880.1:c.28-24G>T NP_001015880.1:n.28-24G>T
NM_004670.3:c.28-24G>T NP_004661.2:n.28-24G>T
NM_001015880.2:c.28-24G>T MANE Select NP_001015880.1:n.28-24G>T
NM_004670.4:c.28-24G>T NP_004661.2:n.28-24G>T