Canonical Allele Identifier: CA34082343

Gene: PTGS2

Linked Data

• dbSNP Id: rs1043850641
• MyVariant Identifiers: chr1:g.186648987G>A (hg19) ; chr1:g.186679855G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186679855G>A , CM000663.2:g.186679855G>A	GRCh38
NC_000001.10:g.186648987G>A , CM000663.1:g.186648987G>A	GRCh37
NC_000001.9:g.184915610G>A	NCBI36
NG_028206.2:g.5573C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367468.10:c.52+384C>T MANE Select	ENSP00000356438.5:n.52+384C>T
ENST00000680451.1:c.52+384C>T	ENSP00000506242.1:n.52+384C>T
ENST00000681605.1:c.52+384C>T	ENSP00000504900.1:n.52+384C>T
ENST00000367468.9:c.52+384C>T	ENSP00000356438.5:n.52+384C>T
ENST00000490885.6:n.185+384C>T
ENST00000559627.1:c.52+384C>T	ENSP00000454130.1:n.52+384C>T
ENST00000559800.1:n.185+384C>T
NM_000963.3:c.52+384C>T	NP_000954.1:n.52+384C>T
NM_000963.4:c.52+384C>T MANE Select	NP_000954.1:n.52+384C>T