Canonical Allele Identifier: CA728758668
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1350060523
MyVariant Identifiers: chr1:g.186642952T>C (hg19) chr1:g.186673820T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673820T>C , CM000663.2:g.186673820T>C GRCh38
NC_000001.10:g.186642952T>C , CM000663.1:g.186642952T>C GRCh37
NC_000001.9:g.184909575T>C NCBI36
NG_028206.2:g.11608A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.*533A>G MANE Select ENSP00000356438.5:n.*533A>G
ENST00000680451.1:c.*533A>G ENSP00000506242.1:n.*533A>G
ENST00000681605.1:c.*2020A>G ENSP00000504900.1:n.*2020A>G
ENST00000367468.9:c.*533A>G ENSP00000356438.5:n.*533A>G
ENST00000490885.6:n.2763A>G
NM_000963.3:c.*533A>G NP_000954.1:n.*533A>G
NM_000963.4:c.*533A>G MANE Select NP_000954.1:n.*533A>G
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