Canonical Allele Identifier: CA274549006

Gene: POLG

Linked Data

• dbSNP Id: rs982596020
• gnomAD v2: 15-89866355-C-A
• gnomAD v3: 15-89323124-C-A
• gnomAD v4: 15-89323124-C-A
• MyVariant Identifiers: chr15:g.89866355C>A (hg19) ; chr15:g.89866355_89866358delinsAATA (hg19) ; chr15:g.89323124C>A (hg38) ; chr15:g.89323124_89323127delinsAATA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89323124C>A , CM000677.2:g.89323124C>A	GRCh38
NC_000015.9:g.89866355C>A , CM000677.1:g.89866355C>A	GRCh37
NC_000015.8:g.87667359C>A	NCBI36
NG_008218.1:g.16672G>T
NG_008218.2:g.16672G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2266-222G>T	ENSP00000516154.1:n.2266-222G>T
ENST00000268124.11:c.2266-222G>T MANE Select	ENSP00000268124.5:n.2266-222G>T
ENST00000530292.3:c.1867-222G>T	ENSP00000432885.2:n.1867-222G>T
ENST00000635986.2:c.2266-222G>T	ENSP00000490653.2:n.2266-222G>T
ENST00000636774.1:c.*833-222G>T	ENSP00000489799.1:n.*833-222G>T
ENST00000637238.1:c.963-222G>T	ENSP00000490756.1:n.963-222G>T
ENST00000637264.1:c.1338-222G>T
ENST00000666746.1:c.1843-222G>T
ENST00000670281.1:c.586-222G>T	ENSP00000499709.1:n.586-222G>T
ENST00000672071.1:n.2464-222G>T
ENST00000672923.2:n.2368+280G>T
ENST00000268124.9:c.2266-222G>T	ENSP00000268124.5:n.2266-222G>T
ENST00000442287.6:c.2266-222G>T	ENSP00000399851.2:n.2266-222G>T
ENST00000526314.2:c.540-222G>T
ENST00000526398.1:c.415-222G>T
ENST00000528881.2:c.35-222G>T
ENST00000530715.5:c.25-222G>T	ENSP00000431395.1:n.25-222G>T
ENST00000532584.5:n.467+280G>T
ENST00000631044.2:c.*1690-222G>T	ENSP00000486730.1:n.*1690-222G>T
NM_001126131.1:c.2266-222G>T	NP_001119603.1:n.2266-222G>T
NM_002693.2:c.2266-222G>T	NP_002684.1:n.2266-222G>T
NM_001126131.2:c.2266-222G>T	NP_001119603.1:n.2266-222G>T
NM_002693.3:c.2266-222G>T MANE Select	NP_002684.1:n.2266-222G>T