Canonical Allele Identifier: CA2581701441
Gene: PTGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-186673903-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673903T>A , CM000663.2:g.186673903T>A GRCh38
NC_000001.10:g.186643035T>A , CM000663.1:g.186643035T>A GRCh37
NC_000001.9:g.184909658T>A NCBI36
NG_028206.2:g.11525A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.*450A>T MANE Select ENSP00000356438.5:n.*450A>T
ENST00000680451.1:c.*450A>T ENSP00000506242.1:n.*450A>T
ENST00000681605.1:c.*1937A>T ENSP00000504900.1:n.*1937A>T
ENST00000367468.9:c.*450A>T ENSP00000356438.5:n.*450A>T
ENST00000490885.6:n.2680A>T
NM_000963.3:c.*450A>T NP_000954.1:n.*450A>T
NM_000963.4:c.*450A>T MANE Select NP_000954.1:n.*450A>T
Search 100 bp 5'
Search 100 bp 3'