Canonical Allele Identifier: CA14190579

Gene: POLG

Linked Data

• ClinVar Variation Id: 1195429
• ClinVar RCV Id: RCV001558506
• dbSNP Id: rs2074884
• gnomAD v2: 15-89864753-C-T
• gnomAD v3: 15-89321522-C-T
• gnomAD v4: 15-89321522-C-T
• MyVariant Identifiers: chr15:g.89864753C>T (hg19) ; chr15:g.89321522C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89321522C>T , CM000677.2:g.89321522C>T	GRCh38
NC_000015.9:g.89864753C>T , CM000677.1:g.89864753C>T	GRCh37
NC_000015.8:g.87665757C>T	NCBI36
NG_008218.1:g.18274G>A
NG_008218.2:g.18274G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.2598+214G>A	ENSP00000516154.1:n.2598+214G>A
ENST00000268124.11:c.2598+214G>A MANE Select	ENSP00000268124.5:n.2598+214G>A
ENST00000530292.3:c.2199+214G>A	ENSP00000432885.2:n.2199+214G>A
ENST00000635986.2:c.2598+214G>A	ENSP00000490653.2:n.2598+214G>A
ENST00000636774.1:c.*1165+214G>A	ENSP00000489799.1:n.*1165+214G>A
ENST00000637238.1:c.1295+214G>A	ENSP00000490756.1:n.1295+214G>A
ENST00000637264.1:c.1670+214G>A
ENST00000666746.1:c.2175+214G>A
ENST00000670281.1:c.800+440G>A	ENSP00000499709.1:n.800+440G>A
ENST00000672071.1:n.2796+214G>A
ENST00000672923.2:n.2540+214G>A
ENST00000268124.9:c.2598+214G>A	ENSP00000268124.5:n.2598+214G>A
ENST00000442287.6:c.2598+214G>A	ENSP00000399851.2:n.2598+214G>A
ENST00000528881.2:c.196-262G>A
ENST00000530715.5:c.186-653G>A	ENSP00000431395.1:n.186-653G>A
ENST00000631044.2:c.*2022+214G>A	ENSP00000486730.1:n.*2022+214G>A
NM_001126131.1:c.2598+214G>A	NP_001119603.1:n.2598+214G>A
NM_002693.2:c.2598+214G>A	NP_002684.1:n.2598+214G>A
NM_001126131.2:c.2598+214G>A	NP_001119603.1:n.2598+214G>A
NM_002693.3:c.2598+214G>A MANE Select	NP_002684.1:n.2598+214G>A