Canonical Allele Identifier: CA344062793

Gene: PTGS2

Linked Data

• gnomAD v4: 1-186680284-C-T
• MyVariant Identifiers: chr1:g.186649416C>T (hg19) ; chr1:g.186680284C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186680284C>T , CM000663.2:g.186680284C>T	GRCh38
NC_000001.10:g.186649416C>T , CM000663.1:g.186649416C>T	GRCh37
NC_000001.9:g.184916039C>T	NCBI36
NG_028206.2:g.5144G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367468.10:c.7G>A MANE Select	ENSP00000356438.5:p.Ala3Thr
ENST00000680451.1:c.7G>A	ENSP00000506242.1:p.Ala3Thr
ENST00000681605.1:c.7G>A	ENSP00000504900.1:p.Ala3Thr
ENST00000367468.9:c.7G>A	ENSP00000356438.5:p.Ala3Thr
ENST00000490885.6:n.140G>A
ENST00000559627.1:c.7G>A	ENSP00000454130.1:p.Ala3Thr
ENST00000559800.1:n.140G>A
NM_000963.3:c.7G>A	NP_000954.1:p.Ala3Thr
NM_000963.4:c.7G>A MANE Select	NP_000954.1:p.Ala3Thr