Canonical Allele Identifier: CA377489486

Gene: PAPSS2

Linked Data

• dbSNP Id: rs1589439333
• MyVariant Identifiers: chr10:g.89487145A>G (hg19) ; chr10:g.87727388A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87727388A>G , CM000672.2:g.87727388A>G	GRCh38
NC_000010.10:g.89487145A>G , CM000672.1:g.89487145A>G	GRCh37
NC_000010.9:g.89477125A>G	NCBI36
NG_012150.1:g.72670A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.985A>G MANE Select	ENSP00000406157.1:p.Arg329Gly
ENST00000361175.8:c.970A>G	ENSP00000354436.4:p.Arg324Gly
ENST00000456849.1:c.985A>G	ENSP00000406157.1:p.Arg329Gly
NM_001015880.1:c.985A>G	NP_001015880.1:p.Arg329Gly
NM_004670.3:c.970A>G	NP_004661.2:p.Arg324Gly
NM_001015880.2:c.985A>G MANE Select	NP_001015880.1:p.Arg329Gly
NM_004670.4:c.970A>G	NP_004661.2:p.Arg324Gly