Canonical Allele Identifier: CA1926080769

Gene: PAPSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87727326C= , CM000672.2:g.87727326C=	GRCh38
NC_000010.10:g.89487083C= , CM000672.1:g.89487083C=	GRCh37
NC_000010.9:g.89477063C=	NCBI36
NG_012150.1:g.72608C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.923C= MANE Select	ENSP00000406157.1:p.Ser308=
ENST00000361175.8:c.908C=	ENSP00000354436.4:p.Ser303=
ENST00000456849.1:c.923C=	ENSP00000406157.1:p.Ser308=
NM_001015880.1:c.923C=	NP_001015880.1:p.Ser308=
NM_004670.3:c.908C=	NP_004661.2:p.Ser303=
NM_001015880.2:c.923C= MANE Select	NP_001015880.1:p.Ser308=
NM_004670.4:c.908C=	NP_004661.2:p.Ser303=