Canonical Allele Identifier: CA15104167
Gene: PTGS2 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.186676356A>G
GRCh37 chr1:g.186645488A>G
gnomAD v2:
1:186645488 A / G
gnomAD v3:
1:186676356 A / G
gnomAD v4:
chr1-186676356-A-G
Joint Max Group AF 0.16285124 (MID)
Genomes Max Group AF 0.13228839 (AMR)
Exomes Max Group AF 0.16176299 (MID)
dbSNP:
4648276
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186676356A>G , CM000663.2:g.186676356A>G GRCh38
NC_000001.10:g.186645488A>G , CM000663.1:g.186645488A>G GRCh37
NC_000001.9:g.184912111A>G NCBI36
NG_028206.2:g.9072T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367468.10:c.970+111T>C MANE Select ENSP00000356438.5:n.970+111T>C
ENST00000680451.1:c.970+111T>C ENSP00000506242.1:n.970+111T>C
ENST00000681605.1:c.*642+111T>C ENSP00000504900.1:n.*642+111T>C
ENST00000367468.9:c.970+111T>C ENSP00000356438.5:n.970+111T>C
ENST00000490885.6:n.1214T>C
ENST00000559627.1:c.860+111T>C ENSP00000454130.1:n.860+111T>C
NM_000963.3:c.970+111T>C NP_000954.1:n.970+111T>C
NM_000963.4:c.970+111T>C MANE Select NP_000954.1:n.970+111T>C
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