Canonical Allele Identifier: CA274549766

Gene: POLG

Linked Data

• dbSNP Id: rs1045255970
• gnomAD v3: 15-89323611-T-C
• gnomAD v4: 15-89323611-T-C
• MyVariant Identifiers: chr15:g.89866842T>C (hg19) ; chr15:g.89323611T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89323611T>C , CM000677.2:g.89323611T>C	GRCh38
NC_000015.9:g.89866842T>C , CM000677.1:g.89866842T>C	GRCh37
NC_000015.8:g.87667846T>C	NCBI36
NG_008218.1:g.16185A>G
NG_008218.2:g.16185A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2158-100A>G	ENSP00000516154.1:n.2158-100A>G
ENST00000268124.11:c.2158-100A>G MANE Select	ENSP00000268124.5:n.2158-100A>G
ENST00000530292.3:c.1759-100A>G	ENSP00000432885.2:n.1759-100A>G
ENST00000635986.2:c.2158-100A>G	ENSP00000490653.2:n.2158-100A>G
ENST00000636774.1:c.*725-100A>G	ENSP00000489799.1:n.*725-100A>G
ENST00000637238.1:c.855-100A>G	ENSP00000490756.1:n.855-100A>G
ENST00000637264.1:c.1230-100A>G
ENST00000666746.1:c.1735-100A>G
ENST00000670281.1:c.478-100A>G	ENSP00000499709.1:n.478-100A>G
ENST00000672071.1:n.2356-100A>G
ENST00000672923.2:n.2261-100A>G
ENST00000268124.9:c.2158-100A>G	ENSP00000268124.5:n.2158-100A>G
ENST00000442287.6:c.2158-100A>G	ENSP00000399851.2:n.2158-100A>G
ENST00000526314.2:c.539+204A>G
ENST00000526398.1:c.307-100A>G
ENST00000526573.1:n.447A>G
ENST00000532584.5:n.360-100A>G
ENST00000533857.1:n.476A>G
ENST00000631044.2:c.*1541-59A>G	ENSP00000486730.1:n.*1541-59A>G
NM_001126131.1:c.2158-100A>G	NP_001119603.1:n.2158-100A>G
NM_002693.2:c.2158-100A>G	NP_002684.1:n.2158-100A>G
NM_001126131.2:c.2158-100A>G	NP_001119603.1:n.2158-100A>G
NM_002693.3:c.2158-100A>G MANE Select	NP_002684.1:n.2158-100A>G