Canonical Allele Identifier: CA728763077
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1161417788
MyVariant Identifiers: chr1:g.186648936del (hg19) chr1:g.186679804del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186679805del , CM000663.2:g.186679805del GRCh38
NC_000001.10:g.186648937del , CM000663.1:g.186648937del GRCh37
NC_000001.9:g.184915560del NCBI36
NG_028206.2:g.5624del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.53-366del MANE Select ENSP00000356438.5:n.53-366del
ENST00000680451.1:c.53-366del ENSP00000506242.1:n.53-366del
ENST00000681605.1:c.53-366del ENSP00000504900.1:n.53-366del
ENST00000367468.9:c.53-366del ENSP00000356438.5:n.53-366del
ENST00000490885.6:n.186-366del
ENST00000559627.1:c.53-366del ENSP00000454130.1:n.53-366del
ENST00000559800.1:n.186-366del
NM_000963.3:c.53-366del NP_000954.1:n.53-366del
NM_000963.4:c.53-366del MANE Select NP_000954.1:n.53-366del
Search 100 bp 5'
Search 100 bp 3'