Canonical Allele Identifier: CA1139774318

Gene: PTGS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186680288C= , CM000663.2:g.186680288C=	GRCh38
NC_000001.10:g.186649420C= , CM000663.1:g.186649420C=	GRCh37
NC_000001.9:g.184916043C=	NCBI36
NG_028206.2:g.5140G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367468.10:c.3G= MANE Select	ENSP00000356438.5:p.Met1=
ENST00000680451.1:c.3G=	ENSP00000506242.1:p.Met1=
ENST00000681605.1:c.3G=	ENSP00000504900.1:p.Met1=
ENST00000367468.9:c.3G=	ENSP00000356438.5:p.Met1=
ENST00000490885.6:n.136G=
ENST00000559627.1:c.3G=	ENSP00000454130.1:p.Met1=
ENST00000559800.1:n.136G=
NM_000963.3:c.3G=	NP_000954.1:p.Met1=
NM_000963.4:c.3G= MANE Select	NP_000954.1:p.Met1=