Canonical Allele Identifier: CA422373908
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs1363215691
MyVariant Identifiers: chr1:g.186649863T>C (hg19) chr1:g.186680731T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680731T>C , CM000663.2:g.186680731T>C GRCh38
NC_000001.10:g.186649863T>C , CM000663.1:g.186649863T>C GRCh37
NC_000001.9:g.184916486T>C NCBI36
NG_028206.2:g.4697A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-141A>G (PTGS2) ENSP00000506242.1:n.-141A>G
NR_125801.1:n.78T>C (PACERR)
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