Canonical Allele Identifier: CA7725001

Gene: POLG

Linked Data

• ClinVar Variation Id: 1425375
• ClinVar RCV Id: RCV001957402
• dbSNP Id: rs749799663
• ExAC: 15:89872290 C / T
• gnomAD v2: 15-89872290-C-T
• gnomAD v3: 15-89329059-C-T
• gnomAD v4: 15-89329059-C-T
• MyVariant Identifiers: chr15:g.89872290C>T (hg19) ; chr15:g.89329059C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89329059C>T , CM000677.2:g.89329059C>T	GRCh38
NC_000015.9:g.89872290C>T , CM000677.1:g.89872290C>T	GRCh37
NC_000015.8:g.87673294C>T	NCBI36
NG_008218.1:g.10737G>A
NG_008218.2:g.10737G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.907G>A	ENSP00000516154.1:p.Gly303Arg
ENST00000268124.11:c.907G>A MANE Select	ENSP00000268124.5:p.Gly303Arg
ENST00000530292.3:c.508G>A	ENSP00000432885.2:p.Gly170Arg
ENST00000635986.2:c.907G>A	ENSP00000490653.2:p.Gly303Arg
ENST00000636774.1:c.907G>A	ENSP00000489799.1:p.Gly303Arg
ENST00000666746.1:c.564G>A
ENST00000672071.1:n.1105G>A
ENST00000268124.9:c.907G>A	ENSP00000268124.5:p.Gly303Arg
ENST00000442287.6:c.907G>A	ENSP00000399851.2:p.Gly303Arg
ENST00000631044.2:c.*290G>A	ENSP00000486730.1:n.*290G>A
NM_001126131.1:c.907G>A	NP_001119603.1:p.Gly303Arg
NM_002693.2:c.907G>A	NP_002684.1:p.Gly303Arg
NM_001126131.2:c.907G>A	NP_001119603.1:p.Gly303Arg
NM_002693.3:c.907G>A MANE Select	NP_002684.1:p.Gly303Arg