Canonical Allele Identifier: CA1213243963

Gene: PTGS2

Linked Data

• dbSNP Id: rs1665732735

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186673825dup , CM000663.2:g.186673825dup	GRCh38
NC_000001.10:g.186642957dup , CM000663.1:g.186642957dup	GRCh37
NC_000001.9:g.184909580dup	NCBI36
NG_028206.2:g.11604dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367468.10:c.*529dup MANE Select	ENSP00000356438.5:n.*529dup
ENST00000680451.1:c.*529dup	ENSP00000506242.1:n.*529dup
ENST00000681605.1:c.*2016dup	ENSP00000504900.1:n.*2016dup
ENST00000367468.9:c.*529dup	ENSP00000356438.5:n.*529dup
ENST00000490885.6:n.2759dup
NM_000963.3:c.*529dup	NP_000954.1:n.*529dup
NM_000963.4:c.*529dup MANE Select	NP_000954.1:n.*529dup