Canonical Allele Identifier: CA14173996
Gene: POLG HGNC NCBI
POLGARF HGNC NCBI

Linked Data

dbSNP Id: rs2238296

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89332098A>G , CM000677.2:g.89332098A>G GRCh38
NC_000015.9:g.89875329A>G , CM000677.1:g.89875329A>G GRCh37
NC_000015.8:g.87676333A>G NCBI36
NG_008218.1:g.7698T>C
NG_008218.2:g.7698T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000636937.2:c.659+998T>C (POLG) ENSP00000516154.1:n.659+998T>C
ENST00000706918.1:c.714+998T>C (POLGARF) ENSP00000516626.1:n.714+998T>C
ENST00000268124.11:c.659+998T>C (POLG) MANE Select ENSP00000268124.5:n.659+998T>C
ENST00000530292.3:c.260+998T>C (POLG) ENSP00000432885.2:n.260+998T>C
ENST00000635986.2:c.659+998T>C (POLG) ENSP00000490653.2:n.659+998T>C
ENST00000636774.1:c.659+998T>C (POLG) ENSP00000489799.1:n.659+998T>C
ENST00000637307.1:c.49+998T>C (POLG)
ENST00000650303.2:c.714+998T>C (POLG) ENSP00000497242.2:n.714+998T>C
ENST00000666746.1:c.316+998T>C (POLG)
ENST00000672071.1:n.857+998T>C (POLG)
ENST00000268124.9:c.659+998T>C (POLG) ENSP00000268124.5:n.659+998T>C
ENST00000442287.6:c.659+998T>C (POLG) ENSP00000399851.2:n.659+998T>C
ENST00000631044.2:c.*42+120T>C (POLG) ENSP00000486730.1:n.*42+120T>C
NM_001126131.1:c.659+998T>C (POLG) NP_001119603.1:n.659+998T>C
NM_002693.2:c.659+998T>C (POLG) NP_002684.1:n.659+998T>C
NM_001126131.2:c.659+998T>C (POLG) NP_001119603.1:n.659+998T>C
NM_002693.3:c.659+998T>C (POLG) MANE Select NP_002684.1:n.659+998T>C