Canonical Allele Identifier: CA344062807

Gene: PTGS2

Linked Data

• MyVariant Identifiers: chr1:g.186649422T>C (hg19) ; chr1:g.186680290T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186680290T>C , CM000663.2:g.186680290T>C	GRCh38
NC_000001.10:g.186649422T>C , CM000663.1:g.186649422T>C	GRCh37
NC_000001.9:g.184916045T>C	NCBI36
NG_028206.2:g.5138A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367468.10:c.1A>G MANE Select	ENSP00000356438.5:p.Met1Val
ENST00000680451.1:c.1A>G	ENSP00000506242.1:p.Met1Val
ENST00000681605.1:c.1A>G	ENSP00000504900.1:p.Met1Val
ENST00000367468.9:c.1A>G	ENSP00000356438.5:p.Met1Val
ENST00000490885.6:n.134A>G
ENST00000559627.1:c.1A>G	ENSP00000454130.1:p.Met1Val
ENST00000559800.1:n.134A>G
NM_000963.3:c.1A>G	NP_000954.1:p.Met1Val
NM_000963.4:c.1A>G MANE Select	NP_000954.1:p.Met1Val