Canonical Allele Identifier: CA527762151

Gene: PTGS2

Linked Data

• dbSNP Id: rs1373484287
• gnomAD v2: 1-186643009-T-G
• gnomAD v3: 1-186673877-T-G
• gnomAD v4: 1-186673877-T-G
• MyVariant Identifiers: chr1:g.186643009T>G (hg19) ; chr1:g.186673877T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186673877T>G , CM000663.2:g.186673877T>G	GRCh38
NC_000001.10:g.186643009T>G , CM000663.1:g.186643009T>G	GRCh37
NC_000001.9:g.184909632T>G	NCBI36
NG_028206.2:g.11551A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367468.10:c.*476A>C MANE Select	ENSP00000356438.5:n.*476A>C
ENST00000680451.1:c.*476A>C	ENSP00000506242.1:n.*476A>C
ENST00000681605.1:c.*1963A>C	ENSP00000504900.1:n.*1963A>C
ENST00000367468.9:c.*476A>C	ENSP00000356438.5:n.*476A>C
ENST00000490885.6:n.2706A>C
NM_000963.3:c.*476A>C	NP_000954.1:n.*476A>C
NM_000963.4:c.*476A>C MANE Select	NP_000954.1:n.*476A>C