Canonical Allele Identifier: CA34081576

Gene: PTGS2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186672065C>T , CM000663.2:g.186672065C>T	GRCh38
NC_000001.10:g.186641197C>T , CM000663.1:g.186641197C>T	GRCh37
NC_000001.9:g.184907820C>T	NCBI36
NG_028206.2:g.13363G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367468.10:c.*2288G>A MANE Select	ENSP00000356438.5:n.*2288G>A
ENST00000680451.1:c.*2288G>A	ENSP00000506242.1:n.*2288G>A
ENST00000681605.1:c.*3775G>A	ENSP00000504900.1:n.*3775G>A
ENST00000367468.9:c.*2288G>A	ENSP00000356438.5:n.*2288G>A
NM_000963.3:c.*2288G>A	NP_000954.1:n.*2288G>A
NM_000963.4:c.*2288G>A MANE Select	NP_000954.1:n.*2288G>A