Canonical Allele Identifier: CA422374270
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.186649975C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680843C>T , CM000663.2:g.186680843C>T GRCh38
NC_000001.10:g.186649975C>T , CM000663.1:g.186649975C>T GRCh37
NC_000001.9:g.184916598C>T NCBI36
NG_028206.2:g.4585G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-253G>A (PTGS2) ENSP00000506242.1:n.-253G>A
NR_125801.1:n.190C>T (PACERR)