Canonical Allele Identifier: CA2610038257

Gene: PAPSS2

Linked Data

• gnomAD v4: 10-87727508-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87727508G>T , CM000672.2:g.87727508G>T	GRCh38
NC_000010.10:g.89487265G>T , CM000672.1:g.89487265G>T	GRCh37
NC_000010.9:g.89477245G>T	NCBI36
NG_012150.1:g.72790G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456849.2:c.1086+19G>T MANE Select	ENSP00000406157.1:n.1086+19G>T
ENST00000361175.8:c.1071+19G>T	ENSP00000354436.4:n.1071+19G>T
ENST00000456849.1:c.1086+19G>T	ENSP00000406157.1:n.1086+19G>T
NM_001015880.1:c.1086+19G>T	NP_001015880.1:n.1086+19G>T
NM_004670.3:c.1071+19G>T	NP_004661.2:n.1071+19G>T
NM_001015880.2:c.1086+19G>T MANE Select	NP_001015880.1:n.1086+19G>T
NM_004670.4:c.1071+19G>T	NP_004661.2:n.1071+19G>T