Canonical Allele Identifier: CA7725003

Gene: POLG

Linked Data

• dbSNP Id: rs774932187
• ExAC: 15:89872295 A / G
• gnomAD v2: 15-89872295-A-G
• gnomAD v4: 15-89329064-A-G
• MyVariant Identifiers: chr15:g.89872295A>G (hg19) ; chr15:g.89329064A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89329064A>G , CM000677.2:g.89329064A>G	GRCh38
NC_000015.9:g.89872295A>G , CM000677.1:g.89872295A>G	GRCh37
NC_000015.8:g.87673299A>G	NCBI36
NG_008218.1:g.10732T>C
NG_008218.2:g.10732T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.902T>C	ENSP00000516154.1:p.Ile301Thr
ENST00000268124.11:c.902T>C MANE Select	ENSP00000268124.5:p.Ile301Thr
ENST00000530292.3:c.503T>C	ENSP00000432885.2:p.Ile168Thr
ENST00000635986.2:c.902T>C	ENSP00000490653.2:p.Ile301Thr
ENST00000636774.1:c.902T>C	ENSP00000489799.1:p.Ile301Thr
ENST00000666746.1:c.559T>C
ENST00000672071.1:n.1100T>C
ENST00000268124.9:c.902T>C	ENSP00000268124.5:p.Ile301Thr
ENST00000442287.6:c.902T>C	ENSP00000399851.2:p.Ile301Thr
ENST00000631044.2:c.*285T>C	ENSP00000486730.1:n.*285T>C
NM_001126131.1:c.902T>C	NP_001119603.1:p.Ile301Thr
NM_002693.2:c.902T>C	NP_002684.1:p.Ile301Thr
NM_001126131.2:c.902T>C	NP_001119603.1:p.Ile301Thr
NM_002693.3:c.902T>C MANE Select	NP_002684.1:p.Ile301Thr