Canonical Allele Identifier: CA2606348940
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs2102004181
gnomAD v3: 1-186673819-T-C
gnomAD v4: 1-186673819-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673819T>C , CM000663.2:g.186673819T>C GRCh38
NC_000001.10:g.186642951T>C , CM000663.1:g.186642951T>C GRCh37
NC_000001.9:g.184909574T>C NCBI36
NG_028206.2:g.11609A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.*534A>G MANE Select ENSP00000356438.5:n.*534A>G
ENST00000680451.1:c.*534A>G ENSP00000506242.1:n.*534A>G
ENST00000681605.1:c.*2021A>G ENSP00000504900.1:n.*2021A>G
ENST00000367468.9:c.*534A>G ENSP00000356438.5:n.*534A>G
ENST00000490885.6:n.2764A>G
NM_000963.3:c.*534A>G NP_000954.1:n.*534A>G
NM_000963.4:c.*534A>G MANE Select NP_000954.1:n.*534A>G
Search 100 bp 5'
Search 100 bp 3'