Canonical Allele Identifier: CA34082416
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs981604329
gnomAD v4: 1-186680351-T-C
MyVariant Identifiers: chr1:g.186649483T>C (hg19) chr1:g.186680351T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680351T>C , CM000663.2:g.186680351T>C GRCh38
NC_000001.10:g.186649483T>C , CM000663.1:g.186649483T>C GRCh37
NC_000001.9:g.184916106T>C NCBI36
NG_028206.2:g.5077A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.-61A>G MANE Select ENSP00000356438.5:n.-61A>G
ENST00000680451.1:c.-61A>G ENSP00000506242.1:n.-61A>G
ENST00000681605.1:c.-61A>G ENSP00000504900.1:n.-61A>G
ENST00000367468.9:c.-61A>G ENSP00000356438.5:n.-61A>G
ENST00000490885.6:n.73A>G
ENST00000559800.1:n.73A>G
NM_000963.3:c.-61A>G NP_000954.1:n.-61A>G
NM_000963.4:c.-61A>G MANE Select NP_000954.1:n.-61A>G
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