Canonical Allele Identifier: CA10602291

Gene: POLG POLGARF

Linked Data

• ClinVar Variation Id: 619379
• ClinVar RCV Id: RCV000758391
• dbSNP Id: rs1028326668
• gnomAD v2: 15-89876470-C-T
• gnomAD v3: 15-89333239-C-T
• gnomAD v4: 15-89333239-C-T
• MyVariant Identifiers: chr15:g.89876470C>T (hg19) ; chr15:g.89333239C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89333239C>T , CM000677.2:g.89333239C>T	GRCh38
NC_000015.9:g.89876470C>T , CM000677.1:g.89876470C>T	GRCh37
NC_000015.8:g.87677474C>T	NCBI36
NG_008218.1:g.6557G>A
NG_008218.2:g.6557G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.516G>A (POLG)	ENSP00000516154.1:p.Ala172=
ENST00000706918.1:c.571G>A (POLGARF)	ENSP00000516626.1:p.Gly191Arg
ENST00000268124.11:c.516G>A (POLG) MANE Select	ENSP00000268124.5:p.Ala172=
ENST00000530292.3:c.117G>A (POLG)	ENSP00000432885.2:p.Ala39=
ENST00000635986.2:c.516G>A (POLG)	ENSP00000490653.2:p.Ala172=
ENST00000636774.1:c.516G>A (POLG)	ENSP00000489799.1:p.Ala172=
ENST00000650303.2:c.571G>A (POLG)	ENSP00000497242.2:p.Gly191Arg
ENST00000666746.1:c.173G>A (POLG)
ENST00000672071.1:n.714G>A (POLG)
ENST00000268124.9:c.516G>A (POLG)	ENSP00000268124.5:p.Ala172=
ENST00000442287.6:c.516G>A (POLG)	ENSP00000399851.2:p.Ala172=
ENST00000631044.2:c.516G>A (POLG)	ENSP00000486730.1:p.Ala172=
NM_001126131.1:c.516G>A (POLG)	NP_001119603.1:p.Ala172=
NM_002693.2:c.516G>A (POLG)	NP_002684.1:p.Ala172=
NM_001126131.2:c.516G>A (POLG)	NP_001119603.1:p.Ala172=
NM_002693.3:c.516G>A (POLG) MANE Select	NP_002684.1:p.Ala172=