Canonical Allele Identifier: CA7724773
Gene: POLG HGNC NCBI
MIR6766 HGNC NCBI

Linked Data

dbSNP Id: rs778308582

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89326810T>C , CM000677.2:g.89326810T>C GRCh38
NC_000015.9:g.89870041T>C , CM000677.1:g.89870041T>C GRCh37
NC_000015.8:g.87671045T>C NCBI36
NG_008218.1:g.12986A>G
NG_008218.2:g.12986A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.1586-72A>G (POLG) ENSP00000516154.1:n.1586-72A>G
ENST00000268124.11:c.1586-72A>G (POLG) MANE Select ENSP00000268124.5:n.1586-72A>G
ENST00000530292.3:c.1187-72A>G (POLG) ENSP00000432885.2:n.1187-72A>G
ENST00000635986.2:c.1586-72A>G (POLG) ENSP00000490653.2:n.1586-72A>G
ENST00000636774.1:c.*153-72A>G (POLG) ENSP00000489799.1:n.*153-72A>G
ENST00000637238.1:c.323-72A>G (POLG) ENSP00000490756.1:n.323-72A>G
ENST00000637264.1:c.658-72A>G (POLG)
ENST00000666746.1:c.1163-72A>G (POLG)
ENST00000672071.1:n.1784-72A>G (POLG)
ENST00000672923.2:n.1689-72A>G (POLG)
ENST00000268124.9:c.1586-72A>G (POLG) ENSP00000268124.5:n.1586-72A>G
ENST00000442287.6:c.1586-72A>G (POLG) ENSP00000399851.2:n.1586-72A>G
ENST00000631044.2:c.*969-72A>G (POLG) ENSP00000486730.1:n.*969-72A>G
NM_001126131.1:c.1586-72A>G (POLG) NP_001119603.1:n.1586-72A>G
NM_002693.2:c.1586-72A>G (POLG) NP_002684.1:n.1586-72A>G
NR_106824.1:n.1A>G (MIR6766)
NM_001126131.2:c.1586-72A>G (POLG) NP_001119603.1:n.1586-72A>G
NM_002693.3:c.1586-72A>G (POLG) MANE Select NP_002684.1:n.1586-72A>G