Canonical Allele Identifier: CA2531070010

Gene: PTGS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186673787T>C , CM000663.2:g.186673787T>C	GRCh38
NC_000001.10:g.186642919T>C , CM000663.1:g.186642919T>C	GRCh37
NC_000001.9:g.184909542T>C	NCBI36
NG_028206.2:g.11641A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367468.10:c.*566A>G MANE Select	ENSP00000356438.5:n.*566A>G
ENST00000680451.1:c.*566A>G	ENSP00000506242.1:n.*566A>G
ENST00000681605.1:c.*2053A>G	ENSP00000504900.1:n.*2053A>G
ENST00000367468.9:c.*566A>G	ENSP00000356438.5:n.*566A>G
ENST00000490885.6:n.2796A>G
NM_000963.3:c.*566A>G	NP_000954.1:n.*566A>G
NM_000963.4:c.*566A>G MANE Select	NP_000954.1:n.*566A>G