Canonical Allele Identifier: CA2574602747
Gene: PAPSS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727269T>G , CM000672.2:g.87727269T>G GRCh38
NC_000010.10:g.89487026T>G , CM000672.1:g.89487026T>G GRCh37
NC_000010.9:g.89477006T>G NCBI36
NG_012150.1:g.72551T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.881-15T>G MANE Select ENSP00000406157.1:n.881-15T>G
ENST00000361175.8:c.866-15T>G ENSP00000354436.4:n.866-15T>G
ENST00000456849.1:c.881-15T>G ENSP00000406157.1:n.881-15T>G
NM_001015880.1:c.881-15T>G NP_001015880.1:n.881-15T>G
NM_004670.3:c.866-15T>G NP_004661.2:n.866-15T>G
NM_001015880.2:c.881-15T>G MANE Select NP_001015880.1:n.881-15T>G
NM_004670.4:c.866-15T>G NP_004661.2:n.866-15T>G