Canonical Allele Identifier: CA422374389
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

gnomAD v4: 1-186680885-G-A
MyVariant Identifiers: chr1:g.186650017G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680885G>A , CM000663.2:g.186680885G>A GRCh38
NC_000001.10:g.186650017G>A , CM000663.1:g.186650017G>A GRCh37
NC_000001.9:g.184916640G>A NCBI36
NG_028206.2:g.4543C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-295C>T (PTGS2) ENSP00000506242.1:n.-295C>T
NR_125801.1:n.232G>A (PACERR)
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