Canonical Allele Identifier: CA344062808

Gene: PTGS2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367468.10:c.1A>C MANE Select	ENSP00000356438.5:p.Met1Leu
ENST00000680451.1:c.1A>C	ENSP00000506242.1:p.Met1Leu
ENST00000681605.1:c.1A>C	ENSP00000504900.1:p.Met1Leu
ENST00000367468.9:c.1A>C	ENSP00000356438.5:p.Met1Leu
ENST00000490885.6:n.134A>C
ENST00000559627.1:c.1A>C	ENSP00000454130.1:p.Met1Leu
ENST00000559800.1:n.134A>C
NM_000963.3:c.1A>C	NP_000954.1:p.Met1Leu
NM_000963.4:c.1A>C MANE Select	NP_000954.1:p.Met1Leu