Canonical Allele Identifier: CA728763452
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1250867207
gnomAD v4: 1-186680607-C-A
MyVariant Identifiers: chr1:g.186649739C>A (hg19) chr1:g.186680607C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680607C>A , CM000663.2:g.186680607C>A GRCh38
NC_000001.10:g.186649739C>A , CM000663.1:g.186649739C>A GRCh37
NC_000001.9:g.184916362C>A NCBI36
NG_028206.2:g.4821G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-114+97G>T ENSP00000506242.1:n.-114+97G>T
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