Canonical Allele Identifier: CA470667986
Gene: PAPSS2 HGNC NCBI

Linked Data

dbSNP Id: rs762509625
gnomAD v2: 10-89487042-T-C
gnomAD v3: 10-87727285-T-C
gnomAD v4: 10-87727285-T-C
MyVariant Identifiers: chr10:g.89487042T>C (hg19) chr10:g.87727285T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727285T>C , CM000672.2:g.87727285T>C GRCh38
NC_000010.10:g.89487042T>C , CM000672.1:g.89487042T>C GRCh37
NC_000010.9:g.89477022T>C NCBI36
NG_012150.1:g.72567T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.882T>C MANE Select ENSP00000406157.1:p.Asp294=
ENST00000361175.8:c.867T>C ENSP00000354436.4:p.Asp289=
ENST00000456849.1:c.882T>C ENSP00000406157.1:p.Asp294=
NM_001015880.1:c.882T>C NP_001015880.1:p.Asp294=
NM_004670.3:c.867T>C NP_004661.2:p.Asp289=
NM_001015880.2:c.882T>C MANE Select NP_001015880.1:p.Asp294=
NM_004670.4:c.867T>C NP_004661.2:p.Asp289=
Search 100 bp 5'
Search 100 bp 3'