Canonical Allele Identifier: CA344062797
Gene: PTGS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680286A>C , CM000663.2:g.186680286A>C GRCh38
NC_000001.10:g.186649418A>C , CM000663.1:g.186649418A>C GRCh37
NC_000001.9:g.184916041A>C NCBI36
NG_028206.2:g.5142T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.5T>G MANE Select ENSP00000356438.5:p.Leu2Arg
ENST00000680451.1:c.5T>G ENSP00000506242.1:p.Leu2Arg
ENST00000681605.1:c.5T>G ENSP00000504900.1:p.Leu2Arg
ENST00000367468.9:c.5T>G ENSP00000356438.5:p.Leu2Arg
ENST00000490885.6:n.138T>G
ENST00000559627.1:c.5T>G ENSP00000454130.1:p.Leu2Arg
ENST00000559800.1:n.138T>G
NM_000963.3:c.5T>G NP_000954.1:p.Leu2Arg
NM_000963.4:c.5T>G MANE Select NP_000954.1:p.Leu2Arg