Canonical Allele Identifier: CA467190935

Gene: PTGS1

Linked Data

• dbSNP Id: rs907158454
• gnomAD v2: 9-125143720-C-T
• gnomAD v4: 9-122381441-C-T
• MyVariant Identifiers: chr9:g.125143720C>T (hg19) ; chr9:g.122381441C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122381441C>T , CM000671.2:g.122381441C>T	GRCh38
NC_000009.11:g.125143720C>T , CM000671.1:g.125143720C>T	GRCh37
NC_000009.10:g.124183541C>T	NCBI36
NG_032900.1:g.15492C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000362012.7:c.567C>T MANE Select	ENSP00000354612.2:p.Asp189=
ENST00000373698.7:c.240C>T	ENSP00000362802.5:p.Asp80=
ENST00000426608.6:c.313-55C>T	ENSP00000411606.2:n.313-55C>T
ENST00000540753.6:c.492C>T	ENSP00000437709.1:p.Asp164=
ENST00000619306.5:c.423C>T	ENSP00000483540.2:p.Asp141=
ENST00000643576.1:n.661C>T
ENST00000643810.1:c.240C>T	ENSP00000494717.1:p.Asp80=
ENST00000645132.1:n.519+2868C>T
ENST00000647067.1:c.*412C>T	ENSP00000495728.1:n.*412C>T
ENST00000223423.8:c.567C>T	ENSP00000223423.4:p.Asp189=
ENST00000362012.6:c.567C>T	ENSP00000354612.2:p.Asp189=
ENST00000373698.6:c.240C>T	ENSP00000362802.5:p.Asp80=
ENST00000426608.5:c.304-55C>T	ENSP00000411606.1:n.304-55C>T
ENST00000540753.5:c.492C>T	ENSP00000437709.1:p.Asp164=
ENST00000614910.4:c.423C>T	ENSP00000484800.1:p.Asp141=
ENST00000619306.4:c.660C>T	ENSP00000483540.1:p.Asp220=
NM_000962.3:c.567C>T	NP_000953.2:p.Asp189=
NM_001271164.1:c.423C>T	NP_001258093.1:p.Asp141=
NM_001271165.1:c.240C>T	NP_001258094.1:p.Asp80=
NM_001271166.1:c.240C>T	NP_001258095.1:p.Asp80=
NM_001271367.1:c.240C>T	NP_001258296.1:p.Asp80=
NM_001271368.1:c.492C>T	NP_001258297.1:p.Asp164=
NM_080591.2:c.567C>T	NP_542158.1:p.Asp189=
XM_005252105.2:c.492C>T	XP_005252162.1:p.Asp164=
XM_011518875.1:c.492C>T	XP_011517177.1:p.Asp164=
XM_011518876.1:c.240C>T	XP_011517178.1:p.Asp80=
XM_005252105.3:c.492C>T	XP_005252162.1:p.Asp164=
XM_011518875.2:c.492C>T	XP_011517177.1:p.Asp164=
XM_011518876.2:c.240C>T	XP_011517178.1:p.Asp80=
XM_024447614.1:c.240C>T	XP_024303382.1:p.Asp80=
XM_024447615.1:c.240C>T	XP_024303383.1:p.Asp80=
NM_000962.4:c.567C>T MANE Select	NP_000953.2:p.Asp189=
NM_001271164.2:c.423C>T	NP_001258093.1:p.Asp141=
NM_001271165.2:c.240C>T	NP_001258094.1:p.Asp80=
NM_001271166.2:c.240C>T	NP_001258095.1:p.Asp80=
NM_001271367.2:c.240C>T	NP_001258296.1:p.Asp80=
NM_001271368.2:c.492C>T	NP_001258297.1:p.Asp164=
NM_080591.3:c.567C>T	NP_542158.1:p.Asp189=