Canonical Allele Identifier: CA34082435
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs748256782
gnomAD v2: 1-186649626-C-T
gnomAD v3: 1-186680494-C-T
gnomAD v4: 1-186680494-C-T
MyVariant Identifiers: chr1:g.186649626C>T (hg19) chr1:g.186680494C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680494C>T , CM000663.2:g.186680494C>T GRCh38
NC_000001.10:g.186649626C>T , CM000663.1:g.186649626C>T GRCh37
NC_000001.9:g.184916249C>T NCBI36
NG_028206.2:g.4934G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-113-91G>A ENSP00000506242.1:n.-113-91G>A
Search 100 bp 5'
Search 100 bp 3'