Canonical Allele Identifier: CA2649581957
Gene: PTGS2 HGNC NCBI

Linked Data

gnomAD v4: 1-186673909-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673909T>C , CM000663.2:g.186673909T>C GRCh38
NC_000001.10:g.186643041T>C , CM000663.1:g.186643041T>C GRCh37
NC_000001.9:g.184909664T>C NCBI36
NG_028206.2:g.11519A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.*444A>G MANE Select ENSP00000356438.5:n.*444A>G
ENST00000680451.1:c.*444A>G ENSP00000506242.1:n.*444A>G
ENST00000681605.1:c.*1931A>G ENSP00000504900.1:n.*1931A>G
ENST00000367468.9:c.*444A>G ENSP00000356438.5:n.*444A>G
ENST00000490885.6:n.2674A>G
NM_000963.3:c.*444A>G NP_000954.1:n.*444A>G
NM_000963.4:c.*444A>G MANE Select NP_000954.1:n.*444A>G
Search 100 bp 5'
Search 100 bp 3'