Canonical Allele Identifier: CA422374061
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.186649909C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680777C>G , CM000663.2:g.186680777C>G GRCh38
NC_000001.10:g.186649909C>G , CM000663.1:g.186649909C>G GRCh37
NC_000001.9:g.184916532C>G NCBI36
NG_028206.2:g.4651G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-187G>C (PTGS2) ENSP00000506242.1:n.-187G>C
NR_125801.1:n.124C>G (PACERR)