Canonical Allele Identifier: CA211271659
Gene: PAPSS2 HGNC NCBI

Linked Data

dbSNP Id: rs768759177
gnomAD v2: 10-89487051-C-A
gnomAD v3: 10-87727294-C-A
gnomAD v4: 10-87727294-C-A
MyVariant Identifiers: chr10:g.89487051C>A (hg19) chr10:g.87727294C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727294C>A , CM000672.2:g.87727294C>A GRCh38
NC_000010.10:g.89487051C>A , CM000672.1:g.89487051C>A GRCh37
NC_000010.9:g.89477031C>A NCBI36
NG_012150.1:g.72576C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.891C>A MANE Select ENSP00000406157.1:p.Ile297=
ENST00000361175.8:c.876C>A ENSP00000354436.4:p.Ile292=
ENST00000456849.1:c.891C>A ENSP00000406157.1:p.Ile297=
NM_001015880.1:c.891C>A NP_001015880.1:p.Ile297=
NM_004670.3:c.876C>A NP_004661.2:p.Ile292=
NM_001015880.2:c.891C>A MANE Select NP_001015880.1:p.Ile297=
NM_004670.4:c.876C>A NP_004661.2:p.Ile292=
Search 100 bp 5'
Search 100 bp 3'