Canonical Allele Identifier: CA1926063578
Gene: PAPSS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727478C= , CM000672.2:g.87727478C= GRCh38
NC_000010.10:g.89487235C= , CM000672.1:g.89487235C= GRCh37
NC_000010.9:g.89477215C= NCBI36
NG_012150.1:g.72760C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.1075C= MANE Select ENSP00000406157.1:p.Pro359=
ENST00000361175.8:c.1060C= ENSP00000354436.4:p.Pro354=
ENST00000456849.1:c.1075C= ENSP00000406157.1:p.Pro359=
NM_001015880.1:c.1075C= NP_001015880.1:p.Pro359=
NM_004670.3:c.1060C= NP_004661.2:p.Pro354=
NM_001015880.2:c.1075C= MANE Select NP_001015880.1:p.Pro359=
NM_004670.4:c.1060C= NP_004661.2:p.Pro354=