Canonical Allele Identifier: CA916359515

Gene: PTGS2

Linked Data

• dbSNP Id: rs1553255950

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186680293del , CM000663.2:g.186680293del	GRCh38
NC_000001.10:g.186649425del , CM000663.1:g.186649425del	GRCh37
NC_000001.9:g.184916048del	NCBI36
NG_028206.2:g.5135del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367468.10:c.-3del MANE Select	ENSP00000356438.5:n.-3del
ENST00000680451.1:c.-3del	ENSP00000506242.1:n.-3del
ENST00000681605.1:c.-3del	ENSP00000504900.1:n.-3del
ENST00000367468.9:c.-3del	ENSP00000356438.5:n.-3del
ENST00000490885.6:n.131del
ENST00000559800.1:n.131del
NM_000963.3:c.-3del	NP_000954.1:n.-3del
NM_000963.4:c.-3del MANE Select	NP_000954.1:n.-3del