Canonical Allele Identifier: CA422374155
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs1665868855
MyVariant Identifiers: chr1:g.186649937A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680805A>C , CM000663.2:g.186680805A>C GRCh38
NC_000001.10:g.186649937A>C , CM000663.1:g.186649937A>C GRCh37
NC_000001.9:g.184916560A>C NCBI36
NG_028206.2:g.4623T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-215T>G (PTGS2) ENSP00000506242.1:n.-215T>G
NR_125801.1:n.152A>C (PACERR)