Canonical Allele Identifier: CA1299588
Gene: PTGS2 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.186676795C>T
GRCh37 chr1:g.186645927C>T
gnomAD v2:
1:186645927 C / T
gnomAD v3:
1:186676795 C / T
gnomAD v4:
chr1-186676795-C-T
Joint Max Group AF 0.32493081 (AFR)
Genomes Max Group AF 0.32203289 (AFR)
Exomes Max Group AF 0.32537378 (AFR)
dbSNP:
2066826
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186676795C>T , CM000663.2:g.186676795C>T GRCh38
NC_000001.10:g.186645927C>T , CM000663.1:g.186645927C>T GRCh37
NC_000001.9:g.184912550C>T NCBI36
NG_028206.2:g.8633G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.723+38G>A MANE Select ENSP00000356438.5:n.723+38G>A
ENST00000680451.1:c.723+38G>A ENSP00000506242.1:n.723+38G>A
ENST00000681605.1:c.*395+38G>A ENSP00000504900.1:n.*395+38G>A
ENST00000367468.9:c.723+38G>A ENSP00000356438.5:n.723+38G>A
ENST00000490885.6:n.856+38G>A
ENST00000559627.1:c.613+38G>A ENSP00000454130.1:n.613+38G>A
NM_000963.3:c.723+38G>A NP_000954.1:n.723+38G>A
NM_000963.4:c.723+38G>A MANE Select NP_000954.1:n.723+38G>A
Search 100 bp 5'
Search 100 bp 3'