Canonical Allele Identifier: CA422374272
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

gnomAD v4: 1-186680844-C-A
MyVariant Identifiers: chr1:g.186649976C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680844C>A , CM000663.2:g.186680844C>A GRCh38
NC_000001.10:g.186649976C>A , CM000663.1:g.186649976C>A GRCh37
NC_000001.9:g.184916599C>A NCBI36
NG_028206.2:g.4584G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-254G>T (PTGS2) ENSP00000506242.1:n.-254G>T
NR_125801.1:n.191C>A (PACERR)
Search 100 bp 5'
Search 100 bp 3'