Canonical Allele Identifier: CA422373964
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.186649880G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680748G>C , CM000663.2:g.186680748G>C GRCh38
NC_000001.10:g.186649880G>C , CM000663.1:g.186649880G>C GRCh37
NC_000001.9:g.184916503G>C NCBI36
NG_028206.2:g.4680C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-158C>G (PTGS2) ENSP00000506242.1:n.-158C>G
NR_125801.1:n.95G>C (PACERR)