Canonical Allele Identifier: CA2649583200

Gene: PTGS2

Linked Data

• gnomAD v4: 1-186680357-TGAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186680359_186680361del , CM000663.2:g.186680359_186680361del	GRCh38
NC_000001.10:g.186649491_186649493del , CM000663.1:g.186649491_186649493del	GRCh37
NC_000001.9:g.184916114_184916116del	NCBI36
NG_028206.2:g.5068_5070del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367468.10:c.-70_-68del MANE Select	ENSP00000356438.5:n.-70_-68del
ENST00000680451.1:c.-70_-68del	ENSP00000506242.1:n.-70_-68del
ENST00000681605.1:c.-70_-68del	ENSP00000504900.1:n.-70_-68del
ENST00000367468.9:c.-70_-68del	ENSP00000356438.5:n.-70_-68del
ENST00000490885.6:n.64_66del
ENST00000559800.1:n.64_66del
NM_000963.3:c.-70_-68del	NP_000954.1:n.-70_-68del
NM_000963.4:c.-70_-68del MANE Select	NP_000954.1:n.-70_-68del