Canonical Allele Identifier: CA34082428

Gene: PTGS2

Linked Data

• dbSNP Id: rs5271
• gnomAD v2: 1-186649547-A-C
• gnomAD v3: 1-186680415-A-C
• gnomAD v4: 1-186680415-A-C
• MyVariant Identifiers: chr1:g.186649547A>C (hg19) ; chr1:g.186680415A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186680415A>C , CM000663.2:g.186680415A>C	GRCh38
NC_000001.10:g.186649547A>C , CM000663.1:g.186649547A>C	GRCh37
NC_000001.9:g.184916170A>C	NCBI36
NG_028206.2:g.5013T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367468.10:c.-125T>G MANE Select	ENSP00000356438.5:n.-125T>G
ENST00000680451.1:c.-113-12T>G	ENSP00000506242.1:n.-113-12T>G
ENST00000681605.1:c.-125T>G	ENSP00000504900.1:n.-125T>G
ENST00000367468.9:c.-125T>G	ENSP00000356438.5:n.-125T>G
ENST00000490885.6:n.9T>G
ENST00000559800.1:n.9T>G
NM_000963.3:c.-125T>G	NP_000954.1:n.-125T>G
NM_000963.4:c.-125T>G MANE Select	NP_000954.1:n.-125T>G