Canonical Allele Identifier: CA34082452

Gene: PTGS2

Linked Data

• dbSNP Id: rs943639133
• gnomAD v4: 1-186680565-G-A
• MyVariant Identifiers: chr1:g.186649697G>A (hg19) ; chr1:g.186680565G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186680565G>A , CM000663.2:g.186680565G>A	GRCh38
NC_000001.10:g.186649697G>A , CM000663.1:g.186649697G>A	GRCh37
NC_000001.9:g.184916320G>A	NCBI36
NG_028206.2:g.4863C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000680451.1:c.-114+139C>T	ENSP00000506242.1:n.-114+139C>T