Canonical Allele Identifier: CA422374405

Gene: PTGS2 PACERR

Linked Data

• dbSNP Id: rs1437053373
• gnomAD v2: 1-186650022-C-G
• gnomAD v3: 1-186680890-C-G
• gnomAD v4: 1-186680890-C-G
• MyVariant Identifiers: chr1:g.186650022C>G (hg19) ; chr1:g.186680890C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186680890C>G , CM000663.2:g.186680890C>G	GRCh38
NC_000001.10:g.186650022C>G , CM000663.1:g.186650022C>G	GRCh37
NC_000001.9:g.184916645C>G	NCBI36
NG_028206.2:g.4538G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000680451.1:c.-300G>C (PTGS2)	ENSP00000506242.1:n.-300G>C
NR_125801.1:n.237C>G (PACERR)