Canonical Allele Identifier: CA422374078
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs1243214592
gnomAD v3: 1-186680782-T-A
gnomAD v4: 1-186680782-T-A
MyVariant Identifiers: chr1:g.186649914T>A (hg19) chr1:g.186680782T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680782T>A , CM000663.2:g.186680782T>A GRCh38
NC_000001.10:g.186649914T>A , CM000663.1:g.186649914T>A GRCh37
NC_000001.9:g.184916537T>A NCBI36
NG_028206.2:g.4646A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-192A>T (PTGS2) ENSP00000506242.1:n.-192A>T
NR_125801.1:n.129T>A (PACERR)
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