Canonical Allele Identifier: CA422373879
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs1299610296
gnomAD v3: 1-186680722-T-A
gnomAD v4: 1-186680722-T-A
MyVariant Identifiers: chr1:g.186649854T>A (hg19) chr1:g.186680722T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680722T>A , CM000663.2:g.186680722T>A GRCh38
NC_000001.10:g.186649854T>A , CM000663.1:g.186649854T>A GRCh37
NC_000001.9:g.184916477T>A NCBI36
NG_028206.2:g.4706A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-132A>T (PTGS2) ENSP00000506242.1:n.-132A>T
NR_125801.1:n.69T>A (PACERR)
Search 100 bp 5'
Search 100 bp 3'