Canonical Allele Identifier: CA2606348931
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs2102003423
gnomAD v3: 1-186672616-C-A
gnomAD v4: 1-186672616-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186672616C>A , CM000663.2:g.186672616C>A GRCh38
NC_000001.10:g.186641748C>A , CM000663.1:g.186641748C>A GRCh37
NC_000001.9:g.184908371C>A NCBI36
NG_028206.2:g.12812G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.*1737G>T MANE Select ENSP00000356438.5:n.*1737G>T
ENST00000680451.1:c.*1737G>T ENSP00000506242.1:n.*1737G>T
ENST00000681605.1:c.*3224G>T ENSP00000504900.1:n.*3224G>T
ENST00000367468.9:c.*1737G>T ENSP00000356438.5:n.*1737G>T
NM_000963.3:c.*1737G>T NP_000954.1:n.*1737G>T
NM_000963.4:c.*1737G>T MANE Select NP_000954.1:n.*1737G>T
Search 100 bp 5'
Search 100 bp 3'