Canonical Allele Identifier: CA377489571
Gene: PAPSS2 HGNC NCBI

Linked Data

dbSNP Id: rs1346300859
gnomAD v2: 10-89487184-A-G
gnomAD v3: 10-87727427-A-G
gnomAD v4: 10-87727427-A-G
MyVariant Identifiers: chr10:g.89487184A>G (hg19) chr10:g.87727427A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727427A>G , CM000672.2:g.87727427A>G GRCh38
NC_000010.10:g.89487184A>G , CM000672.1:g.89487184A>G GRCh37
NC_000010.9:g.89477164A>G NCBI36
NG_012150.1:g.72709A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.1024A>G MANE Select ENSP00000406157.1:p.Arg342Gly
ENST00000361175.8:c.1009A>G ENSP00000354436.4:p.Arg337Gly
ENST00000456849.1:c.1024A>G ENSP00000406157.1:p.Arg342Gly
NM_001015880.1:c.1024A>G NP_001015880.1:p.Arg342Gly
NM_004670.3:c.1009A>G NP_004661.2:p.Arg337Gly
NM_001015880.2:c.1024A>G MANE Select NP_001015880.1:p.Arg342Gly
NM_004670.4:c.1009A>G NP_004661.2:p.Arg337Gly
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