Canonical Allele Identifier: CA2649583137

Gene: PTGS2

Linked Data

• gnomAD v4: 1-186680305-GGGCGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186680313_186680317del , CM000663.2:g.186680313_186680317del	GRCh38
NC_000001.10:g.186649445_186649449del , CM000663.1:g.186649445_186649449del	GRCh37
NC_000001.9:g.184916068_184916072del	NCBI36
NG_028206.2:g.5118_5122del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367468.10:c.-20_-16del MANE Select	ENSP00000356438.5:n.-20_-16del
ENST00000680451.1:c.-20_-16del	ENSP00000506242.1:n.-20_-16del
ENST00000681605.1:c.-20_-16del	ENSP00000504900.1:n.-20_-16del
ENST00000367468.9:c.-20_-16del	ENSP00000356438.5:n.-20_-16del
ENST00000490885.6:n.114_118del
ENST00000559800.1:n.114_118del
NM_000963.3:c.-20_-16del	NP_000954.1:n.-20_-16del
NM_000963.4:c.-20_-16del MANE Select	NP_000954.1:n.-20_-16del