Canonical Allele Identifier: CA470668146
Gene: PAPSS2 HGNC NCBI

Linked Data

gnomAD v4: 10-87727327-T-C
MyVariant Identifiers: chr10:g.89487084T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727327T>C , CM000672.2:g.87727327T>C GRCh38
NC_000010.10:g.89487084T>C , CM000672.1:g.89487084T>C GRCh37
NC_000010.9:g.89477064T>C NCBI36
NG_012150.1:g.72609T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.924T>C MANE Select ENSP00000406157.1:p.Ser308=
ENST00000361175.8:c.909T>C ENSP00000354436.4:p.Ser303=
ENST00000456849.1:c.924T>C ENSP00000406157.1:p.Ser308=
NM_001015880.1:c.924T>C NP_001015880.1:p.Ser308=
NM_004670.3:c.909T>C NP_004661.2:p.Ser303=
NM_001015880.2:c.924T>C MANE Select NP_001015880.1:p.Ser308=
NM_004670.4:c.909T>C NP_004661.2:p.Ser303=
Search 100 bp 5'
Search 100 bp 3'