Canonical Allele Identifier: CA211271895
Gene: PAPSS2 HGNC NCBI

Linked Data

dbSNP Id: rs911725771
gnomAD v4: 10-87727535-T-G
MyVariant Identifiers: chr10:g.89487292T>G (hg19) chr10:g.87727535T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727535T>G , CM000672.2:g.87727535T>G GRCh38
NC_000010.10:g.89487292T>G , CM000672.1:g.89487292T>G GRCh37
NC_000010.9:g.89477272T>G NCBI36
NG_012150.1:g.72817T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.1086+46T>G MANE Select ENSP00000406157.1:n.1086+46T>G
ENST00000361175.8:c.1071+46T>G ENSP00000354436.4:n.1071+46T>G
ENST00000456849.1:c.1086+46T>G ENSP00000406157.1:n.1086+46T>G
NM_001015880.1:c.1086+46T>G NP_001015880.1:n.1086+46T>G
NM_004670.3:c.1071+46T>G NP_004661.2:n.1071+46T>G
NM_001015880.2:c.1086+46T>G MANE Select NP_001015880.1:n.1086+46T>G
NM_004670.4:c.1071+46T>G NP_004661.2:n.1071+46T>G
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