Canonical Allele Identifier: CA619857618
Gene: POLG HGNC NCBI

Linked Data

dbSNP Id: rs1244049865

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89321881G>A , CM000677.2:g.89321881G>A GRCh38
NC_000015.9:g.89865112G>A , CM000677.1:g.89865112G>A GRCh37
NC_000015.8:g.87666116G>A NCBI36
NG_008218.1:g.17915C>T
NG_008218.2:g.17915C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.2481-28C>T ENSP00000516154.1:n.2481-28C>T
ENST00000268124.11:c.2481-28C>T MANE Select ENSP00000268124.5:n.2481-28C>T
ENST00000530292.3:c.2082-28C>T ENSP00000432885.2:n.2082-28C>T
ENST00000635986.2:c.2481-28C>T ENSP00000490653.2:n.2481-28C>T
ENST00000636774.1:c.*1048-28C>T ENSP00000489799.1:n.*1048-28C>T
ENST00000637238.1:c.1178-28C>T ENSP00000490756.1:n.1178-28C>T
ENST00000637264.1:c.1553-28C>T
ENST00000666746.1:c.2058-28C>T
ENST00000670281.1:c.800+81C>T ENSP00000499709.1:n.800+81C>T
ENST00000672071.1:n.2679-28C>T
ENST00000672923.2:n.2423-28C>T
ENST00000268124.9:c.2481-28C>T ENSP00000268124.5:n.2481-28C>T
ENST00000442287.6:c.2481-28C>T ENSP00000399851.2:n.2481-28C>T
ENST00000528881.2:c.196-621C>T
ENST00000530715.5:c.185+861C>T ENSP00000431395.1:n.185+861C>T
ENST00000532584.5:n.602C>T
ENST00000631044.2:c.*1905-28C>T ENSP00000486730.1:n.*1905-28C>T
NM_001126131.1:c.2481-28C>T NP_001119603.1:n.2481-28C>T
NM_002693.2:c.2481-28C>T NP_002684.1:n.2481-28C>T
NM_001126131.2:c.2481-28C>T NP_001119603.1:n.2481-28C>T
NM_002693.3:c.2481-28C>T MANE Select NP_002684.1:n.2481-28C>T