Canonical Allele Identifier: CA2610038255
Gene: PAPSS2 HGNC NCBI

Linked Data

gnomAD v4: 10-87727504-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727504C>A , CM000672.2:g.87727504C>A GRCh38
NC_000010.10:g.89487261C>A , CM000672.1:g.89487261C>A GRCh37
NC_000010.9:g.89477241C>A NCBI36
NG_012150.1:g.72786C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.1086+15C>A MANE Select ENSP00000406157.1:n.1086+15C>A
ENST00000361175.8:c.1071+15C>A ENSP00000354436.4:n.1071+15C>A
ENST00000456849.1:c.1086+15C>A ENSP00000406157.1:n.1086+15C>A
NM_001015880.1:c.1086+15C>A NP_001015880.1:n.1086+15C>A
NM_004670.3:c.1071+15C>A NP_004661.2:n.1071+15C>A
NM_001015880.2:c.1086+15C>A MANE Select NP_001015880.1:n.1086+15C>A
NM_004670.4:c.1071+15C>A NP_004661.2:n.1071+15C>A
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