Canonical Allele Identifier: CA2691549999

Gene: PTGS1

Linked Data

• gnomAD v4: 9-122370792-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.122370792C>T , CM000671.2:g.122370792C>T	GRCh38
NC_000009.11:g.125133071C>T , CM000671.1:g.125133071C>T	GRCh37
NC_000009.10:g.124172892C>T	NCBI36
NG_032900.1:g.4843C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000540753.6:c.-341C>T	ENSP00000437709.1:n.-341C>T
ENST00000643810.1:c.-371C>T	ENSP00000494717.1:n.-371C>T
ENST00000540753.5:c.-341C>T	ENSP00000437709.1:n.-341C>T
NM_001271166.1:c.-371C>T	NP_001258095.1:n.-371C>T
NM_001271368.1:c.-341C>T	NP_001258297.1:n.-341C>T
XM_011518875.1:c.-341C>T	XP_011517177.1:n.-341C>T
XM_011518876.1:c.-4203C>T	XP_011517178.1:n.-4203C>T
XM_011518875.2:c.-341C>T	XP_011517177.1:n.-341C>T
XM_011518876.2:c.-4203C>T	XP_011517178.1:n.-4203C>T
XM_024447614.1:c.-371C>T	XP_024303382.1:n.-371C>T
XM_024447615.1:c.-371C>T	XP_024303383.1:n.-371C>T
NM_001271166.2:c.-371C>T	NP_001258095.1:n.-371C>T
NM_001271368.2:c.-341C>T	NP_001258297.1:n.-341C>T