Canonical Allele Identifier: CA211271667
Gene: PAPSS2 HGNC NCBI

Linked Data

dbSNP Id: rs267602608
gnomAD v2: 10-89487063-C-T
gnomAD v4: 10-87727306-C-T
MyVariant Identifiers: chr10:g.89487063C>T (hg19) chr10:g.87727306C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727306C>T , CM000672.2:g.87727306C>T GRCh38
NC_000010.10:g.89487063C>T , CM000672.1:g.89487063C>T GRCh37
NC_000010.9:g.89477043C>T NCBI36
NG_012150.1:g.72588C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.903C>T MANE Select ENSP00000406157.1:p.Ile301=
ENST00000361175.8:c.888C>T ENSP00000354436.4:p.Ile296=
ENST00000456849.1:c.903C>T ENSP00000406157.1:p.Ile301=
NM_001015880.1:c.903C>T NP_001015880.1:p.Ile301=
NM_004670.3:c.888C>T NP_004661.2:p.Ile296=
NM_001015880.2:c.903C>T MANE Select NP_001015880.1:p.Ile301=
NM_004670.4:c.888C>T NP_004661.2:p.Ile296=
Search 100 bp 5'
Search 100 bp 3'