Canonical Allele Identifier: CA528080522

Gene: PTGS2

Linked Data

• dbSNP Id: rs1451742451
• gnomAD v2: 1-186649679-A-T
• gnomAD v3: 1-186680547-A-T
• gnomAD v4: 1-186680547-A-T
• MyVariant Identifiers: chr1:g.186649679A>T (hg19) ; chr1:g.186680547A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186680547A>T , CM000663.2:g.186680547A>T	GRCh38
NC_000001.10:g.186649679A>T , CM000663.1:g.186649679A>T	GRCh37
NC_000001.9:g.184916302A>T	NCBI36
NG_028206.2:g.4881T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000680451.1:c.-113-144T>A	ENSP00000506242.1:n.-113-144T>A