Canonical Allele Identifier: CA34082445

Gene: PTGS2

Linked Data

• dbSNP Id: rs569072139
• gnomAD v3: 1-186680537-C-G
• gnomAD v4: 1-186680537-C-G
• MyVariant Identifiers: chr1:g.186649669C>G (hg19) ; chr1:g.186680537C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186680537C>G , CM000663.2:g.186680537C>G	GRCh38
NC_000001.10:g.186649669C>G , CM000663.1:g.186649669C>G	GRCh37
NC_000001.9:g.184916292C>G	NCBI36
NG_028206.2:g.4891G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000680451.1:c.-113-134G>C	ENSP00000506242.1:n.-113-134G>C