Canonical Allele Identifier: CA422373905
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs1386758934
MyVariant Identifiers: chr1:g.186649862T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680730T>C , CM000663.2:g.186680730T>C GRCh38
NC_000001.10:g.186649862T>C , CM000663.1:g.186649862T>C GRCh37
NC_000001.9:g.184916485T>C NCBI36
NG_028206.2:g.4698A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-140A>G (PTGS2) ENSP00000506242.1:n.-140A>G
NR_125801.1:n.77T>C (PACERR)