Canonical Allele Identifier: CA2194549134

Gene: POLG

Linked Data

• dbSNP Id: rs2055498152
• gnomAD v4: 15-89325298-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325298G>A , CM000677.2:g.89325298G>A	GRCh38
NC_000015.9:g.89868529G>A , CM000677.1:g.89868529G>A	GRCh37
NC_000015.8:g.87669533G>A	NCBI36
NG_008218.1:g.14498C>T
NG_008218.2:g.14498C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1949+152C>T	ENSP00000516154.1:n.1949+152C>T
ENST00000268124.11:c.1949+152C>T MANE Select	ENSP00000268124.5:n.1949+152C>T
ENST00000530292.3:c.1550+152C>T	ENSP00000432885.2:n.1550+152C>T
ENST00000635986.2:c.1949+152C>T	ENSP00000490653.2:n.1949+152C>T
ENST00000636774.1:c.*516+152C>T	ENSP00000489799.1:n.*516+152C>T
ENST00000637238.1:c.646+192C>T	ENSP00000490756.1:n.646+192C>T
ENST00000637264.1:c.1021+152C>T
ENST00000666746.1:c.1526+152C>T
ENST00000670281.1:c.269+152C>T	ENSP00000499709.1:n.269+152C>T
ENST00000672071.1:n.2147+152C>T
ENST00000672923.2:n.2052+152C>T
ENST00000268124.9:c.1949+152C>T	ENSP00000268124.5:n.1949+152C>T
ENST00000442287.6:c.1949+152C>T	ENSP00000399851.2:n.1949+152C>T
ENST00000526314.2:c.331+152C>T
ENST00000526398.1:c.138+152C>T
ENST00000526573.1:n.35+152C>T
ENST00000532584.5:n.151+152C>T
ENST00000631044.2:c.*1332+152C>T	ENSP00000486730.1:n.*1332+152C>T
NM_001126131.1:c.1949+152C>T	NP_001119603.1:n.1949+152C>T
NM_002693.2:c.1949+152C>T	NP_002684.1:n.1949+152C>T
NM_001126131.2:c.1949+152C>T	NP_001119603.1:n.1949+152C>T
NM_002693.3:c.1949+152C>T MANE Select	NP_002684.1:n.1949+152C>T