Canonical Allele Identifier: CA7724973

Gene: POLG

Linked Data

• dbSNP Id: rs757463848
• ExAC: 15:89872125 G / C
• gnomAD v2: 15-89872125-G-C
• gnomAD v4: 15-89328894-G-C
• MyVariant Identifiers: chr15:g.89872125G>C (hg19) ; chr15:g.89328894G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89328894G>C , CM000677.2:g.89328894G>C	GRCh38
NC_000015.9:g.89872125G>C , CM000677.1:g.89872125G>C	GRCh37
NC_000015.8:g.87673129G>C	NCBI36
NG_008218.1:g.10902C>G
NG_008218.2:g.10902C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.1023+49C>G	ENSP00000516154.1:n.1023+49C>G
ENST00000268124.11:c.1023+49C>G MANE Select	ENSP00000268124.5:n.1023+49C>G
ENST00000530292.3:c.624+49C>G	ENSP00000432885.2:n.624+49C>G
ENST00000635986.2:c.1023+49C>G	ENSP00000490653.2:n.1023+49C>G
ENST00000636774.1:c.1023+49C>G	ENSP00000489799.1:n.1023+49C>G
ENST00000637264.1:c.95+49C>G
ENST00000666746.1:c.680+49C>G
ENST00000672071.1:n.1221+49C>G
ENST00000672923.2:n.20+49C>G
ENST00000268124.9:c.1023+49C>G	ENSP00000268124.5:n.1023+49C>G
ENST00000442287.6:c.1023+49C>G	ENSP00000399851.2:n.1023+49C>G
ENST00000631044.2:c.*406+49C>G	ENSP00000486730.1:n.*406+49C>G
NM_001126131.1:c.1023+49C>G	NP_001119603.1:n.1023+49C>G
NM_002693.2:c.1023+49C>G	NP_002684.1:n.1023+49C>G
NM_001126131.2:c.1023+49C>G	NP_001119603.1:n.1023+49C>G
NM_002693.3:c.1023+49C>G MANE Select	NP_002684.1:n.1023+49C>G