Canonical Allele Identifier: CA2649583033
Gene: PTGS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680283_186680312del , CM000663.2:g.186680283_186680312del GRCh38
NC_000001.10:g.186649415_186649444del , CM000663.1:g.186649415_186649444del GRCh37
NC_000001.9:g.184916038_184916067del NCBI36
NG_028206.2:g.5127_5156del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.-11_19del
ENST00000680451.1:c.-11_19del
ENST00000681605.1:c.-11_19del
ENST00000367468.9:c.-11_19del
ENST00000490885.6:n.123_152del
ENST00000559800.1:n.123_152del
NM_000963.3:c.-11_19del
NM_000963.4:c.-11_19del