Canonical Allele Identifier: CA34082506
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs180835304
gnomAD v2: 1-186650048-G-A
gnomAD v3: 1-186680916-G-A
gnomAD v4: 1-186680916-G-A
MyVariant Identifiers: chr1:g.186650048G>A (hg19) chr1:g.186680916G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680916G>A , CM000663.2:g.186680916G>A GRCh38
NC_000001.10:g.186650048G>A , CM000663.1:g.186650048G>A GRCh37
NC_000001.9:g.184916671G>A NCBI36
NG_028206.2:g.4512C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-326C>T (PTGS2) ENSP00000506242.1:n.-326C>T
NR_125801.1:n.263G>A (PACERR)
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