Canonical Allele Identifier: CA1213245417

Gene: PTGS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186679852T= , CM000663.2:g.186679852T=	GRCh38
NC_000001.10:g.186648984T= , CM000663.1:g.186648984T=	GRCh37
NC_000001.9:g.184915607T=	NCBI36
NG_028206.2:g.5576A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367468.10:c.52+387A= MANE Select	ENSP00000356438.5:n.52+387A=
ENST00000680451.1:c.52+387A=	ENSP00000506242.1:n.52+387A=
ENST00000681605.1:c.52+387A=	ENSP00000504900.1:n.52+387A=
ENST00000367468.9:c.52+387A=	ENSP00000356438.5:n.52+387A=
ENST00000490885.6:n.185+387A=
ENST00000559627.1:c.52+387A=	ENSP00000454130.1:n.52+387A=
ENST00000559800.1:n.185+387A=
NM_000963.3:c.52+387A=	NP_000954.1:n.52+387A=
NM_000963.4:c.52+387A= MANE Select	NP_000954.1:n.52+387A=