Canonical Allele Identifier: CA422374312
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs1364327798
gnomAD v2: 1-186649990-G-A
gnomAD v3: 1-186680858-G-A
gnomAD v4: 1-186680858-G-A
MyVariant Identifiers: chr1:g.186649990G>A (hg19) chr1:g.186680858G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680858G>A , CM000663.2:g.186680858G>A GRCh38
NC_000001.10:g.186649990G>A , CM000663.1:g.186649990G>A GRCh37
NC_000001.9:g.184916613G>A NCBI36
NG_028206.2:g.4570C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-268C>T (PTGS2) ENSP00000506242.1:n.-268C>T
NR_125801.1:n.205G>A (PACERR)
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