Canonical Allele Identifier: CA1299774

Gene: PTGS2

Linked Data

• dbSNP Id: rs3134591
• ExAC: 1:186649425 C / A
• gnomAD v2: 1-186649425-C-A
• gnomAD v4: 1-186680293-C-A
• MyVariant Identifiers: chr1:g.186649425C>A (hg19) ; chr1:g.186680293C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186680293C>A , CM000663.2:g.186680293C>A	GRCh38
NC_000001.10:g.186649425C>A , CM000663.1:g.186649425C>A	GRCh37
NC_000001.9:g.184916048C>A	NCBI36
NG_028206.2:g.5135G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367468.10:c.-3G>T MANE Select	ENSP00000356438.5:n.-3G>T
ENST00000680451.1:c.-3G>T	ENSP00000506242.1:n.-3G>T
ENST00000681605.1:c.-3G>T	ENSP00000504900.1:n.-3G>T
ENST00000367468.9:c.-3G>T	ENSP00000356438.5:n.-3G>T
ENST00000490885.6:n.131G>T
ENST00000559800.1:n.131G>T
NM_000963.3:c.-3G>T	NP_000954.1:n.-3G>T
NM_000963.4:c.-3G>T MANE Select	NP_000954.1:n.-3G>T