Canonical Allele Identifier: CA2649583525

Gene: PTGS2

Linked Data

• gnomAD v4: 1-186679569-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186679575del , CM000663.2:g.186679575del	GRCh38
NC_000001.10:g.186648707del , CM000663.1:g.186648707del	GRCh37
NC_000001.9:g.184915330del	NCBI36
NG_028206.2:g.5858del

Transcript Alleles

HGVS	Amino-acid change
ENST00000367468.10:c.53-132del MANE Select	ENSP00000356438.5:n.53-132del
ENST00000680451.1:c.53-132del	ENSP00000506242.1:n.53-132del
ENST00000681605.1:c.53-132del	ENSP00000504900.1:n.53-132del
ENST00000367468.9:c.53-132del	ENSP00000356438.5:n.53-132del
ENST00000490885.6:n.186-132del
ENST00000559627.1:c.53-132del	ENSP00000454130.1:n.53-132del
ENST00000559800.1:n.186-132del
NM_000963.3:c.53-132del	NP_000954.1:n.53-132del
NM_000963.4:c.53-132del MANE Select	NP_000954.1:n.53-132del