Canonical Allele Identifier: CA34082503

Gene: PTGS2 PACERR

Linked Data

• dbSNP Id: rs1020293874
• gnomAD v3: 1-186680906-G-C
• gnomAD v4: 1-186680906-G-C
• MyVariant Identifiers: chr1:g.186650038G>C (hg19) ; chr1:g.186680906G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186680906G>C , CM000663.2:g.186680906G>C	GRCh38
NC_000001.10:g.186650038G>C , CM000663.1:g.186650038G>C	GRCh37
NC_000001.9:g.184916661G>C	NCBI36
NG_028206.2:g.4522C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000680451.1:c.-316C>G (PTGS2)	ENSP00000506242.1:n.-316C>G
NR_125801.1:n.253G>C (PACERR)