Canonical Allele Identifier: CA2194574076

Gene: POLG POLGARF

Linked Data

• dbSNP Id: rs1596362980

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89333761T>C , CM000677.2:g.89333761T>C	GRCh38
NC_000015.9:g.89876992T>C , CM000677.1:g.89876992T>C	GRCh37
NC_000015.8:g.87677996T>C	NCBI36
NG_008218.1:g.6035A>G
NG_008218.2:g.6035A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000636937.2:c.-7A>G (POLG)	ENSP00000516154.1:n.-7A>G
ENST00000706918.1:c.49A>G (POLGARF)	ENSP00000516626.1:p.Thr17Ala
ENST00000268124.11:c.-7A>G (POLG) MANE Select	ENSP00000268124.5:n.-7A>G
ENST00000635986.2:c.-7A>G (POLG)	ENSP00000490653.2:n.-7A>G
ENST00000636774.1:c.-7A>G (POLG)	ENSP00000489799.1:n.-7A>G
ENST00000650303.2:c.49A>G (POLG)	ENSP00000497242.2:p.Thr17Ala
ENST00000672071.1:n.192A>G (POLG)
ENST00000268124.9:c.-7A>G (POLG)	ENSP00000268124.5:n.-7A>G
ENST00000442287.6:c.-7A>G (POLG)	ENSP00000399851.2:n.-7A>G
ENST00000631044.2:c.-7A>G (POLG)	ENSP00000486730.1:n.-7A>G
NM_001126131.1:c.-7A>G (POLG)	NP_001119603.1:n.-7A>G
NM_002693.2:c.-7A>G (POLG)	NP_002684.1:n.-7A>G
NM_001126131.2:c.-7A>G (POLG)	NP_001119603.1:n.-7A>G
NM_002693.3:c.-7A>G (POLG) MANE Select	NP_002684.1:n.-7A>G