Canonical Allele Identifier: CA15088418

Gene: PTGS2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186673297A>G , CM000663.2:g.186673297A>G	GRCh38
NC_000001.10:g.186642429A>G , CM000663.1:g.186642429A>G	GRCh37
NC_000001.9:g.184909052A>G	NCBI36
NG_028206.2:g.12131T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367468.10:c.*1056T>C MANE Select	ENSP00000356438.5:n.*1056T>C
ENST00000680451.1:c.*1056T>C	ENSP00000506242.1:n.*1056T>C
ENST00000681605.1:c.*2543T>C	ENSP00000504900.1:n.*2543T>C
ENST00000367468.9:c.*1056T>C	ENSP00000356438.5:n.*1056T>C
ENST00000490885.6:n.3286T>C
NM_000963.3:c.*1056T>C	NP_000954.1:n.*1056T>C
NM_000963.4:c.*1056T>C MANE Select	NP_000954.1:n.*1056T>C