Canonical Allele Identifier: CA422374321
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

gnomAD v4: 1-186680861-C-T
MyVariant Identifiers: chr1:g.186649993C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680861C>T , CM000663.2:g.186680861C>T GRCh38
NC_000001.10:g.186649993C>T , CM000663.1:g.186649993C>T GRCh37
NC_000001.9:g.184916616C>T NCBI36
NG_028206.2:g.4567G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-271G>A (PTGS2) ENSP00000506242.1:n.-271G>A
NR_125801.1:n.208C>T (PACERR)
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