Canonical Allele Identifier: CA422374230
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs1665869119
MyVariant Identifiers: chr1:g.186649961A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680829A>C , CM000663.2:g.186680829A>C GRCh38
NC_000001.10:g.186649961A>C , CM000663.1:g.186649961A>C GRCh37
NC_000001.9:g.184916584A>C NCBI36
NG_028206.2:g.4599T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-239T>G (PTGS2) ENSP00000506242.1:n.-239T>G
NR_125801.1:n.176A>C (PACERR)