Canonical Allele Identifier: CA34082499
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs1011305773
gnomAD v3: 1-186680863-G-A
gnomAD v4: 1-186680863-G-A
MyVariant Identifiers: chr1:g.186649995G>A (hg19) chr1:g.186680863G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680863G>A , CM000663.2:g.186680863G>A GRCh38
NC_000001.10:g.186649995G>A , CM000663.1:g.186649995G>A GRCh37
NC_000001.9:g.184916618G>A NCBI36
NG_028206.2:g.4565C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-273C>T (PTGS2) ENSP00000506242.1:n.-273C>T
NR_125801.1:n.210G>A (PACERR)
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