Canonical Allele Identifier: CA470668318

Gene: PAPSS2

Linked Data

• MyVariant Identifiers: chr10:g.89487129G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87727372G>C , CM000672.2:g.87727372G>C	GRCh38
NC_000010.10:g.89487129G>C , CM000672.1:g.89487129G>C	GRCh37
NC_000010.9:g.89477109G>C	NCBI36
NG_012150.1:g.72654G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.969G>C MANE Select	ENSP00000406157.1:p.Leu323=
ENST00000361175.8:c.954G>C	ENSP00000354436.4:p.Leu318=
ENST00000456849.1:c.969G>C	ENSP00000406157.1:p.Leu323=
NM_001015880.1:c.969G>C	NP_001015880.1:p.Leu323=
NM_004670.3:c.954G>C	NP_004661.2:p.Leu318=
NM_001015880.2:c.969G>C MANE Select	NP_001015880.1:p.Leu323=
NM_004670.4:c.954G>C	NP_004661.2:p.Leu318=