Canonical Allele Identifier: CA728763562
Gene: PTGS2 HGNC NCBI
PACERR HGNC NCBI

Linked Data

dbSNP Id: rs1338930360
MyVariant Identifiers: chr1:g.186650037_186650038insGTCTTTAGA (hg19) chr1:g.186680905_186680906insGTCTTTAGA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186680907_186680915dup , CM000663.2:g.186680907_186680915dup GRCh38
NC_000001.10:g.186650039_186650047dup , CM000663.1:g.186650039_186650047dup GRCh37
NC_000001.9:g.184916662_184916670dup NCBI36
NG_028206.2:g.4514_4522dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000680451.1:c.-324_-316dup (PTGS2) ENSP00000506242.1:n.-324_-316dup
NR_125801.1:n.254_262dup (PACERR)
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