Canonical Allele Identifier: CA34082494
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs923267322
gnomAD v2: 1-186649975-C-A
gnomAD v3: 1-186680843-C-A
gnomAD v4: 1-186680843-C-A
MyVariant Identifiers: chr1:g.186649975C>A (hg19) chr1:g.186680843C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680843C>A , CM000663.2:g.186680843C>A GRCh38
NC_000001.10:g.186649975C>A , CM000663.1:g.186649975C>A GRCh37
NC_000001.9:g.184916598C>A NCBI36
NG_028206.2:g.4585G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-253G>T (PTGS2) ENSP00000506242.1:n.-253G>T
NR_125801.1:n.190C>A (PACERR)
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