Canonical Allele Identifier: CA377489416
Gene: PAPSS2 HGNC NCBI

Linked Data

dbSNP Id: rs1376786123

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727355T>G , CM000672.2:g.87727355T>G GRCh38
NC_000010.10:g.89487112T>G , CM000672.1:g.89487112T>G GRCh37
NC_000010.9:g.89477092T>G NCBI36
NG_012150.1:g.72637T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.952T>G MANE Select ENSP00000406157.1:p.Cys318Gly
ENST00000361175.8:c.937T>G ENSP00000354436.4:p.Cys313Gly
ENST00000456849.1:c.952T>G ENSP00000406157.1:p.Cys318Gly
NM_001015880.1:c.952T>G NP_001015880.1:p.Cys318Gly
NM_004670.3:c.937T>G NP_004661.2:p.Cys313Gly
NM_001015880.2:c.952T>G MANE Select NP_001015880.1:p.Cys318Gly
NM_004670.4:c.937T>G NP_004661.2:p.Cys313Gly