Canonical Allele Identifier: CA2194549066

Gene: POLG

Linked Data

• dbSNP Id: rs2055497797

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89325294G>C , CM000677.2:g.89325294G>C	GRCh38
NC_000015.9:g.89868525G>C , CM000677.1:g.89868525G>C	GRCh37
NC_000015.8:g.87669529G>C	NCBI36
NG_008218.1:g.14502C>G
NG_008218.2:g.14502C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1949+156C>G	ENSP00000516154.1:n.1949+156C>G
ENST00000268124.11:c.1949+156C>G MANE Select	ENSP00000268124.5:n.1949+156C>G
ENST00000530292.3:c.1550+156C>G	ENSP00000432885.2:n.1550+156C>G
ENST00000635986.2:c.1949+156C>G	ENSP00000490653.2:n.1949+156C>G
ENST00000636774.1:c.*516+156C>G	ENSP00000489799.1:n.*516+156C>G
ENST00000637238.1:c.646+196C>G	ENSP00000490756.1:n.646+196C>G
ENST00000637264.1:c.1021+156C>G
ENST00000666746.1:c.1526+156C>G
ENST00000670281.1:c.269+156C>G	ENSP00000499709.1:n.269+156C>G
ENST00000672071.1:n.2147+156C>G
ENST00000672923.2:n.2052+156C>G
ENST00000268124.9:c.1949+156C>G	ENSP00000268124.5:n.1949+156C>G
ENST00000442287.6:c.1949+156C>G	ENSP00000399851.2:n.1949+156C>G
ENST00000526314.2:c.331+156C>G
ENST00000526398.1:c.138+156C>G
ENST00000526573.1:n.35+156C>G
ENST00000532584.5:n.151+156C>G
ENST00000631044.2:c.*1332+156C>G	ENSP00000486730.1:n.*1332+156C>G
NM_001126131.1:c.1949+156C>G	NP_001119603.1:n.1949+156C>G
NM_002693.2:c.1949+156C>G	NP_002684.1:n.1949+156C>G
NM_001126131.2:c.1949+156C>G	NP_001119603.1:n.1949+156C>G
NM_002693.3:c.1949+156C>G MANE Select	NP_002684.1:n.1949+156C>G