Canonical Allele Identifier: CA422374060
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs1263710536
gnomAD v4: 1-186680777-C-A
MyVariant Identifiers: chr1:g.186649909C>A (hg19) chr1:g.186680777C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680777C>A , CM000663.2:g.186680777C>A GRCh38
NC_000001.10:g.186649909C>A , CM000663.1:g.186649909C>A GRCh37
NC_000001.9:g.184916532C>A NCBI36
NG_028206.2:g.4651G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-187G>T (PTGS2) ENSP00000506242.1:n.-187G>T
NR_125801.1:n.124C>A (PACERR)
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