Canonical Allele Identifier: CA728758685
Gene: PTGS2 HGNC NCBI

Linked Data

dbSNP Id: rs1486127728
gnomAD v3: 1-186673893-C-G
gnomAD v4: 1-186673893-C-G
MyVariant Identifiers: chr1:g.186643025C>G (hg19) chr1:g.186673893C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186673893C>G , CM000663.2:g.186673893C>G GRCh38
NC_000001.10:g.186643025C>G , CM000663.1:g.186643025C>G GRCh37
NC_000001.9:g.184909648C>G NCBI36
NG_028206.2:g.11535G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367468.10:c.*460G>C MANE Select ENSP00000356438.5:n.*460G>C
ENST00000680451.1:c.*460G>C ENSP00000506242.1:n.*460G>C
ENST00000681605.1:c.*1947G>C ENSP00000504900.1:n.*1947G>C
ENST00000367468.9:c.*460G>C ENSP00000356438.5:n.*460G>C
ENST00000490885.6:n.2690G>C
NM_000963.3:c.*460G>C NP_000954.1:n.*460G>C
NM_000963.4:c.*460G>C MANE Select NP_000954.1:n.*460G>C
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