Canonical Allele Identifier: CA34082411
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs34888870
gnomAD v2: 1-186649447-C-CG
gnomAD v4: 1-186680315-C-CG
MyVariant Identifiers: chr1:g.186649447_186649448insG (hg19) chr1:g.186680315_186680316insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680320dup , CM000663.2:g.186680320dup GRCh38
NC_000001.10:g.186649452dup , CM000663.1:g.186649452dup GRCh37
NC_000001.9:g.184916075dup NCBI36
NG_028206.2:g.5112dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.-26dup MANE Select ENSP00000356438.5:n.-26dup
ENST00000680451.1:c.-26dup ENSP00000506242.1:n.-26dup
ENST00000681605.1:c.-26dup ENSP00000504900.1:n.-26dup
ENST00000367468.9:c.-26dup ENSP00000356438.5:n.-26dup
ENST00000490885.6:n.108dup
ENST00000559800.1:n.108dup
NM_000963.3:c.-26dup NP_000954.1:n.-26dup
NM_000963.4:c.-26dup MANE Select NP_000954.1:n.-26dup
Search 100 bp 5'
Search 100 bp 3'