Canonical Allele Identifier: CA34082318

Gene: PTGS2

Linked Data

• dbSNP Id: rs1055993908
• gnomAD v2: 1-186648681-T-A
• gnomAD v3: 1-186679549-T-A
• gnomAD v4: 1-186679549-T-A
• MyVariant Identifiers: chr1:g.186648681T>A (hg19) ; chr1:g.186679549T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186679549T>A , CM000663.2:g.186679549T>A	GRCh38
NC_000001.10:g.186648681T>A , CM000663.1:g.186648681T>A	GRCh37
NC_000001.9:g.184915304T>A	NCBI36
NG_028206.2:g.5879A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367468.10:c.53-111A>T MANE Select	ENSP00000356438.5:n.53-111A>T
ENST00000680451.1:c.53-111A>T	ENSP00000506242.1:n.53-111A>T
ENST00000681605.1:c.53-111A>T	ENSP00000504900.1:n.53-111A>T
ENST00000367468.9:c.53-111A>T	ENSP00000356438.5:n.53-111A>T
ENST00000490885.6:n.186-111A>T
ENST00000559627.1:c.53-111A>T	ENSP00000454130.1:n.53-111A>T
ENST00000559800.1:n.186-111A>T
NM_000963.3:c.53-111A>T	NP_000954.1:n.53-111A>T
NM_000963.4:c.53-111A>T MANE Select	NP_000954.1:n.53-111A>T