Canonical Allele Identifier: CA1213245599

Gene: PTGS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186680287G= , CM000663.2:g.186680287G=	GRCh38
NC_000001.10:g.186649419G= , CM000663.1:g.186649419G=	GRCh37
NC_000001.9:g.184916042G=	NCBI36
NG_028206.2:g.5141C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367468.10:c.4C= MANE Select	ENSP00000356438.5:p.Leu2=
ENST00000680451.1:c.4C=	ENSP00000506242.1:p.Leu2=
ENST00000681605.1:c.4C=	ENSP00000504900.1:p.Leu2=
ENST00000367468.9:c.4C=	ENSP00000356438.5:p.Leu2=
ENST00000490885.6:n.137C=
ENST00000559627.1:c.4C=	ENSP00000454130.1:p.Leu2=
ENST00000559800.1:n.137C=
NM_000963.3:c.4C=	NP_000954.1:p.Leu2=
NM_000963.4:c.4C= MANE Select	NP_000954.1:p.Leu2=