Canonical Allele Identifier: CA728758664
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs762269568
gnomAD v3: 1-186673771-C-T
gnomAD v4: 1-186673771-C-T
MyVariant Identifiers: chr1:g.186642903C>T (hg19) chr1:g.186673771C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673771C>T , CM000663.2:g.186673771C>T GRCh38
NC_000001.10:g.186642903C>T , CM000663.1:g.186642903C>T GRCh37
NC_000001.9:g.184909526C>T NCBI36
NG_028206.2:g.11657G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.*582G>A MANE Select ENSP00000356438.5:n.*582G>A
ENST00000680451.1:c.*582G>A ENSP00000506242.1:n.*582G>A
ENST00000681605.1:c.*2069G>A ENSP00000504900.1:n.*2069G>A
ENST00000367468.9:c.*582G>A ENSP00000356438.5:n.*582G>A
ENST00000490885.6:n.2812G>A
NM_000963.3:c.*582G>A NP_000954.1:n.*582G>A
NM_000963.4:c.*582G>A MANE Select NP_000954.1:n.*582G>A
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