Canonical Allele Identifier: CA344062795
Gene: PTGS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.186649418A>G (hg19) chr1:g.186680286A>G (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.5T>C MANE Select ENSP00000356438.5:p.Leu2Pro
ENST00000680451.1:c.5T>C ENSP00000506242.1:p.Leu2Pro
ENST00000681605.1:c.5T>C ENSP00000504900.1:p.Leu2Pro
ENST00000367468.9:c.5T>C ENSP00000356438.5:p.Leu2Pro
ENST00000490885.6:n.138T>C
ENST00000559627.1:c.5T>C ENSP00000454130.1:p.Leu2Pro
ENST00000559800.1:n.138T>C
NM_000963.3:c.5T>C NP_000954.1:p.Leu2Pro
NM_000963.4:c.5T>C MANE Select NP_000954.1:p.Leu2Pro
Search 100 bp 5'
Search 100 bp 3'