Canonical Allele Identifier: CA527762145

Gene: PTGS2

Linked Data

• dbSNP Id: rs1290682004
• gnomAD v2: 1-186642961-G-A
• gnomAD v3: 1-186673829-G-A
• gnomAD v4: 1-186673829-G-A
• MyVariant Identifiers: chr1:g.186642961G>A (hg19) ; chr1:g.186673829G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186673829G>A , CM000663.2:g.186673829G>A	GRCh38
NC_000001.10:g.186642961G>A , CM000663.1:g.186642961G>A	GRCh37
NC_000001.9:g.184909584G>A	NCBI36
NG_028206.2:g.11599C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367468.10:c.*524C>T MANE Select	ENSP00000356438.5:n.*524C>T
ENST00000680451.1:c.*524C>T	ENSP00000506242.1:n.*524C>T
ENST00000681605.1:c.*2011C>T	ENSP00000504900.1:n.*2011C>T
ENST00000367468.9:c.*524C>T	ENSP00000356438.5:n.*524C>T
ENST00000490885.6:n.2754C>T
NM_000963.3:c.*524C>T	NP_000954.1:n.*524C>T
NM_000963.4:c.*524C>T MANE Select	NP_000954.1:n.*524C>T