Canonical Allele Identifier: CA2649583198
Gene: PTGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-186680354-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680354A>G , CM000663.2:g.186680354A>G GRCh38
NC_000001.10:g.186649486A>G , CM000663.1:g.186649486A>G GRCh37
NC_000001.9:g.184916109A>G NCBI36
NG_028206.2:g.5074T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.-64T>C MANE Select ENSP00000356438.5:n.-64T>C
ENST00000680451.1:c.-64T>C ENSP00000506242.1:n.-64T>C
ENST00000681605.1:c.-64T>C ENSP00000504900.1:n.-64T>C
ENST00000367468.9:c.-64T>C ENSP00000356438.5:n.-64T>C
ENST00000490885.6:n.70T>C
ENST00000559800.1:n.70T>C
NM_000963.3:c.-64T>C NP_000954.1:n.-64T>C
NM_000963.4:c.-64T>C MANE Select NP_000954.1:n.-64T>C
Search 100 bp 5'
Search 100 bp 3'