Canonical Allele Identifier: CA527766491
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1341205474
gnomAD v2: 1-186649436-A-G
gnomAD v3: 1-186680304-A-G
gnomAD v4: 1-186680304-A-G
MyVariant Identifiers: chr1:g.186649436A>G (hg19) chr1:g.186680304A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680304A>G , CM000663.2:g.186680304A>G GRCh38
NC_000001.10:g.186649436A>G , CM000663.1:g.186649436A>G GRCh37
NC_000001.9:g.184916059A>G NCBI36
NG_028206.2:g.5124T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.-14T>C MANE Select ENSP00000356438.5:n.-14T>C
ENST00000680451.1:c.-14T>C ENSP00000506242.1:n.-14T>C
ENST00000681605.1:c.-14T>C ENSP00000504900.1:n.-14T>C
ENST00000367468.9:c.-14T>C ENSP00000356438.5:n.-14T>C
ENST00000490885.6:n.120T>C
ENST00000559800.1:n.120T>C
NM_000963.3:c.-14T>C NP_000954.1:n.-14T>C
NM_000963.4:c.-14T>C MANE Select NP_000954.1:n.-14T>C
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