Canonical Allele Identifier: CA1213244003
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1665734010
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673909_186673912del , CM000663.2:g.186673909_186673912del GRCh38
NC_000001.10:g.186643041_186643044del , CM000663.1:g.186643041_186643044del GRCh37
NC_000001.9:g.184909664_184909667del NCBI36
NG_028206.2:g.11520_11523del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.*445_*448del MANE Select ENSP00000356438.5:n.*445_*448del
ENST00000680451.1:c.*445_*448del ENSP00000506242.1:n.*445_*448del
ENST00000681605.1:c.*1932_*1935del ENSP00000504900.1:n.*1932_*1935del
ENST00000367468.9:c.*445_*448del ENSP00000356438.5:n.*445_*448del
ENST00000490885.6:n.2675_2678del
NM_000963.3:c.*445_*448del NP_000954.1:n.*445_*448del
NM_000963.4:c.*445_*448del MANE Select NP_000954.1:n.*445_*448del
Search 100 bp 5'
Search 100 bp 3'