Canonical Allele Identifier: CA528080516
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1230475856
gnomAD v2: 1-186649623-T-C
gnomAD v3: 1-186680491-T-C
gnomAD v4: 1-186680491-T-C
MyVariant Identifiers: chr1:g.186649623T>C (hg19) chr1:g.186680491T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680491T>C , CM000663.2:g.186680491T>C GRCh38
NC_000001.10:g.186649623T>C , CM000663.1:g.186649623T>C GRCh37
NC_000001.9:g.184916246T>C NCBI36
NG_028206.2:g.4937A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000680451.1:c.-113-88A>G ENSP00000506242.1:n.-113-88A>G
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