Canonical Allele Identifier: CA422374055
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs1429069935
gnomAD v4: 1-186680775-A-T
MyVariant Identifiers: chr1:g.186649907A>T (hg19) chr1:g.186680775A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680775A>T , CM000663.2:g.186680775A>T GRCh38
NC_000001.10:g.186649907A>T , CM000663.1:g.186649907A>T GRCh37
NC_000001.9:g.184916530A>T NCBI36
NG_028206.2:g.4653T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-185T>A (PTGS2) ENSP00000506242.1:n.-185T>A
NR_125801.1:n.122A>T (PACERR)
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