Canonical Allele Identifier: CA669556503
Gene: PAPSS2 HGNC NCBI

Linked Data

dbSNP Id: rs1254483334
gnomAD v3: 10-87727117-A-AT
gnomAD v4: 10-87727117-A-AT
MyVariant Identifiers: chr10:g.89486874_89486875insT (hg19) chr10:g.87727117_87727118insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87727119dup , CM000672.2:g.87727119dup GRCh38
NC_000010.10:g.89486876dup , CM000672.1:g.89486876dup GRCh37
NC_000010.9:g.89476856dup NCBI36
NG_012150.1:g.72401dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000456849.2:c.881-165dup MANE Select ENSP00000406157.1:n.881-165dup
ENST00000361175.8:c.866-165dup ENSP00000354436.4:n.866-165dup
ENST00000456849.1:c.881-165dup ENSP00000406157.1:n.881-165dup
NM_001015880.1:c.881-165dup NP_001015880.1:n.881-165dup
NM_004670.3:c.866-165dup NP_004661.2:n.866-165dup
NM_001015880.2:c.881-165dup MANE Select NP_001015880.1:n.881-165dup
NM_004670.4:c.866-165dup NP_004661.2:n.866-165dup
Search 100 bp 5'
Search 100 bp 3'