Canonical Allele Identifier: CA1926080792

Gene: PAPSS2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87727379G= , CM000672.2:g.87727379G=	GRCh38
NC_000010.10:g.89487136G= , CM000672.1:g.89487136G=	GRCh37
NC_000010.9:g.89477116G=	NCBI36
NG_012150.1:g.72661G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.976G= MANE Select	ENSP00000406157.1:p.Gly326=
ENST00000361175.8:c.961G=	ENSP00000354436.4:p.Gly321=
ENST00000456849.1:c.976G=	ENSP00000406157.1:p.Gly326=
NM_001015880.1:c.976G=	NP_001015880.1:p.Gly326=
NM_004670.3:c.961G=	NP_004661.2:p.Gly321=
NM_001015880.2:c.976G= MANE Select	NP_001015880.1:p.Gly326=
NM_004670.4:c.961G=	NP_004661.2:p.Gly321=