Canonical Allele Identifier: CA34082457
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1005230348
gnomAD v3: 1-186680592-G-A
gnomAD v4: 1-186680592-G-A
MyVariant Identifiers: chr1:g.186649724G>A (hg19) chr1:g.186680592G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680592G>A , CM000663.2:g.186680592G>A GRCh38
NC_000001.10:g.186649724G>A , CM000663.1:g.186649724G>A GRCh37
NC_000001.9:g.184916347G>A NCBI36
NG_028206.2:g.4836C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-114+112C>T ENSP00000506242.1:n.-114+112C>T
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