Canonical Allele Identifier: CA422374200
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs1300369496
gnomAD v4: 1-186680819-C-A
MyVariant Identifiers: chr1:g.186649951C>A (hg19) chr1:g.186680819C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680819C>A , CM000663.2:g.186680819C>A GRCh38
NC_000001.10:g.186649951C>A , CM000663.1:g.186649951C>A GRCh37
NC_000001.9:g.184916574C>A NCBI36
NG_028206.2:g.4609G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-229G>T (PTGS2) ENSP00000506242.1:n.-229G>T
NR_125801.1:n.166C>A (PACERR)
Search 100 bp 5'
Search 100 bp 3'