Canonical Allele Identifier: CA34081553

Gene: PTGS2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186671926G>T , CM000663.2:g.186671926G>T	GRCh38
NC_000001.10:g.186641058G>T , CM000663.1:g.186641058G>T	GRCh37
NC_000001.9:g.184907681G>T	NCBI36
NG_028206.2:g.13502C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367468.10:c.*2427C>A MANE Select	ENSP00000356438.5:n.*2427C>A
ENST00000680451.1:c.*2427C>A	ENSP00000506242.1:n.*2427C>A
ENST00000681605.1:c.*3914C>A	ENSP00000504900.1:n.*3914C>A
ENST00000367468.9:c.*2427C>A	ENSP00000356438.5:n.*2427C>A
NM_000963.3:c.*2427C>A	NP_000954.1:n.*2427C>A
NM_000963.4:c.*2427C>A MANE Select	NP_000954.1:n.*2427C>A