Canonical Allele Identifier: CA422374113
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

gnomAD v4: 1-186680793-C-T
MyVariant Identifiers: chr1:g.186649925C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680793C>T , CM000663.2:g.186680793C>T GRCh38
NC_000001.10:g.186649925C>T , CM000663.1:g.186649925C>T GRCh37
NC_000001.9:g.184916548C>T NCBI36
NG_028206.2:g.4635G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-203G>A (PTGS2) ENSP00000506242.1:n.-203G>A
NR_125801.1:n.140C>T (PACERR)
Search 100 bp 5'
Search 100 bp 3'