Canonical Allele Identifier: CA422373871
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.186649851G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680719G>C , CM000663.2:g.186680719G>C GRCh38
NC_000001.10:g.186649851G>C , CM000663.1:g.186649851G>C GRCh37
NC_000001.9:g.184916474G>C NCBI36
NG_028206.2:g.4709C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-129C>G (PTGS2) ENSP00000506242.1:n.-129C>G
NR_125801.1:n.66G>C (PACERR)