Canonical Allele Identifier: CA669556499

Gene: PAPSS2

Linked Data

• dbSNP Id: rs1193252110
• MyVariant Identifiers: chr10:g.89486873C>G (hg19) ; chr10:g.87727116C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87727116C>G , CM000672.2:g.87727116C>G	GRCh38
NC_000010.10:g.89486873C>G , CM000672.1:g.89486873C>G	GRCh37
NC_000010.9:g.89476853C>G	NCBI36
NG_012150.1:g.72398C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.881-168C>G MANE Select	ENSP00000406157.1:n.881-168C>G
ENST00000361175.8:c.866-168C>G	ENSP00000354436.4:n.866-168C>G
ENST00000456849.1:c.881-168C>G	ENSP00000406157.1:n.881-168C>G
NM_001015880.1:c.881-168C>G	NP_001015880.1:n.881-168C>G
NM_004670.3:c.866-168C>G	NP_004661.2:n.866-168C>G
NM_001015880.2:c.881-168C>G MANE Select	NP_001015880.1:n.881-168C>G
NM_004670.4:c.866-168C>G	NP_004661.2:n.866-168C>G