Canonical Allele Identifier: CA351714728

Gene: OGG1

Linked Data

• dbSNP Id: rs2077570202
• gnomAD v4: 3-9756535-T-C
• MyVariant Identifiers: chr3:g.9798219T>C (hg19) ; chr3:g.9756535T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9756535T>C , CM000665.2:g.9756535T>C	GRCh38
NC_000003.11:g.9798219T>C , CM000665.1:g.9798219T>C	GRCh37
NC_000003.10:g.9773219T>C	NCBI36
NG_012106.1:g.11592T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302036.12:c.812T>C	ENSP00000306561.7:p.Met271Thr
ENST00000352937.6:c.747+1650T>C	ENSP00000344899.6:n.747+1650T>C
ENST00000707074.1:c.748-232T>C	ENSP00000516725.1:n.748-232T>C
ENST00000344629.12:c.812T>C MANE Select	ENSP00000342851.7:p.Met271Thr
ENST00000302003.11:c.812T>C	ENSP00000305584.7:p.Met271Thr
ENST00000302008.12:c.812T>C	ENSP00000305527.8:p.Met271Thr
ENST00000302036.11:c.812T>C	ENSP00000306561.7:p.Met271Thr
ENST00000339511.9:c.812T>C	ENSP00000345520.5:p.Met271Thr
ENST00000344629.11:c.812T>C	ENSP00000342851.7:p.Met271Thr
ENST00000349503.9:c.747+1650T>C	ENSP00000303132.6:n.747+1650T>C
ENST00000352937.5:c.463+1650T>C
ENST00000383825.2:n.48-232T>C
ENST00000383826.9:c.565+4586T>C	ENSP00000373337.5:n.565+4586T>C
ENST00000416333.1:c.112T>C
ENST00000425665.1:c.*43T>C	ENSP00000396034.1:n.*43T>C
ENST00000426518.5:c.294+4586T>C
ENST00000429146.5:c.562T>C
ENST00000441094.5:c.505T>C
ENST00000449570.6:c.812T>C	ENSP00000403598.2:p.Met271Thr
NM_002542.5:c.812T>C	NP_002533.1:p.Met271Thr
NM_016819.3:c.812T>C	NP_058212.1:p.Met271Thr
NM_016820.3:c.812T>C	NP_058213.1:p.Met271Thr
NM_016821.2:c.812T>C	NP_058214.1:p.Met271Thr
NM_016826.2:c.747+1650T>C	NP_058434.1:n.747+1650T>C
NM_016827.2:c.565+4586T>C	NP_058436.1:n.565+4586T>C
NM_016828.2:c.812T>C	NP_058437.1:p.Met271Thr
NM_016829.2:c.812T>C	NP_058438.1:p.Met271Thr
XM_011533760.1:c.812T>C	XP_011532062.1:p.Met271Thr
NM_001354648.1:c.566-232T>C	NP_001341577.1:n.566-232T>C
NM_001354649.1:c.566-232T>C	NP_001341578.1:n.566-232T>C
NM_001354650.1:c.748-232T>C	NP_001341579.1:n.748-232T>C
NM_001354651.1:c.812T>C	NP_001341580.1:p.Met271Thr
NM_001354652.1:c.748-232T>C	NP_001341581.1:n.748-232T>C
NR_148930.1:n.907T>C
NR_148931.1:n.545T>C
NR_148932.1:n.973T>C
XM_011533760.2:c.812T>C	XP_011532062.1:p.Met271Thr
XM_017006493.2:c.748-232T>C	XP_016861982.1:n.748-232T>C
XM_017006494.2:c.748-232T>C	XP_016861983.1:n.748-232T>C
XM_017006495.2:c.748-232T>C	XP_016861984.1:n.748-232T>C
XM_017006496.2:c.812T>C	XP_016861985.1:p.Met271Thr
XM_017006497.2:c.748-232T>C	XP_016861986.1:n.748-232T>C
XM_017006499.2:c.748-232T>C	XP_016861988.1:n.748-232T>C
XR_001740156.2:n.1116T>C
NM_001354648.2:c.566-232T>C	NP_001341577.1:n.566-232T>C
NM_001354649.2:c.566-232T>C	NP_001341578.1:n.566-232T>C
NM_001354650.2:c.748-232T>C	NP_001341579.1:n.748-232T>C
NM_001354651.2:c.812T>C	NP_001341580.1:p.Met271Thr
NM_001354652.2:c.748-232T>C	NP_001341581.1:n.748-232T>C
NM_002542.6:c.812T>C MANE Select	NP_002533.1:p.Met271Thr
NM_016819.4:c.812T>C	NP_058212.1:p.Met271Thr
NM_016820.4:c.812T>C	NP_058213.1:p.Met271Thr
NM_016821.3:c.812T>C	NP_058214.1:p.Met271Thr
NM_016826.3:c.747+1650T>C	NP_058434.1:n.747+1650T>C
NM_016827.3:c.565+4586T>C	NP_058436.1:n.565+4586T>C
NM_016828.3:c.812T>C	NP_058437.1:p.Met271Thr
NM_016829.3:c.812T>C	NP_058438.1:p.Met271Thr
NR_148930.2:n.899T>C
NR_148931.2:n.537T>C
NR_148932.2:n.965T>C