Canonical Allele Identifier: CA2539193473

Gene: PTGS2

Linked Data

• gnomAD v4: 1-186673902-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186673907del , CM000663.2:g.186673907del	GRCh38
NC_000001.10:g.186643039del , CM000663.1:g.186643039del	GRCh37
NC_000001.9:g.184909662del	NCBI36
NG_028206.2:g.11525del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367468.10:c.*450del MANE Select	ENSP00000356438.5:n.*450del
ENST00000680451.1:c.*450del	ENSP00000506242.1:n.*450del
ENST00000681605.1:c.*1937del	ENSP00000504900.1:n.*1937del
ENST00000367468.9:c.*450del	ENSP00000356438.5:n.*450del
ENST00000490885.6:n.2680del
NM_000963.3:c.*450del	NP_000954.1:n.*450del
NM_000963.4:c.*450del MANE Select	NP_000954.1:n.*450del