Canonical Allele Identifier: CA728758655
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1156824509
MyVariant Identifiers: chr1:g.186642884_186642885insT (hg19) chr1:g.186673752_186673753insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673755dup , CM000663.2:g.186673755dup GRCh38
NC_000001.10:g.186642887dup , CM000663.1:g.186642887dup GRCh37
NC_000001.9:g.184909510dup NCBI36
NG_028206.2:g.11675dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.*600dup MANE Select ENSP00000356438.5:n.*600dup
ENST00000680451.1:c.*600dup ENSP00000506242.1:n.*600dup
ENST00000681605.1:c.*2087dup ENSP00000504900.1:n.*2087dup
ENST00000367468.9:c.*600dup ENSP00000356438.5:n.*600dup
ENST00000490885.6:n.2830dup
NM_000963.3:c.*600dup NP_000954.1:n.*600dup
NM_000963.4:c.*600dup MANE Select NP_000954.1:n.*600dup
Search 100 bp 5'
Search 100 bp 3'