Canonical Allele Identifier: CA492289882

Gene: POLG POLGARF

Linked Data

• dbSNP Id: rs1159974816
• gnomAD v2: 15-89876362-G-A
• gnomAD v4: 15-89333131-G-A
• MyVariant Identifiers: chr15:g.89876362G>A (hg19) ; chr15:g.89333131G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89333131G>A , CM000677.2:g.89333131G>A	GRCh38
NC_000015.9:g.89876362G>A , CM000677.1:g.89876362G>A	GRCh37
NC_000015.8:g.87677366G>A	NCBI36
NG_008218.1:g.6665C>T
NG_008218.2:g.6665C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636937.2:c.624C>T (POLG)	ENSP00000516154.1:p.Cys208=
ENST00000706918.1:c.679C>T (POLGARF)	ENSP00000516626.1:p.Pro227Ser
ENST00000268124.11:c.624C>T (POLG) MANE Select	ENSP00000268124.5:p.Cys208=
ENST00000530292.3:c.225C>T (POLG)	ENSP00000432885.2:p.Cys75=
ENST00000635986.2:c.624C>T (POLG)	ENSP00000490653.2:p.Cys208=
ENST00000636774.1:c.624C>T (POLG)	ENSP00000489799.1:p.Cys208=
ENST00000637307.1:c.14C>T (POLG)
ENST00000650303.2:c.679C>T (POLG)	ENSP00000497242.2:p.Pro227Ser
ENST00000666746.1:c.281C>T (POLG)
ENST00000672071.1:n.822C>T (POLG)
ENST00000268124.9:c.624C>T (POLG)	ENSP00000268124.5:p.Cys208=
ENST00000442287.6:c.624C>T (POLG)	ENSP00000399851.2:p.Cys208=
ENST00000631044.2:c.624C>T (POLG)	ENSP00000486730.1:p.Cys208=
NM_001126131.1:c.624C>T (POLG)	NP_001119603.1:p.Cys208=
NM_002693.2:c.624C>T (POLG)	NP_002684.1:p.Cys208=
NM_001126131.2:c.624C>T (POLG)	NP_001119603.1:p.Cys208=
NM_002693.3:c.624C>T (POLG) MANE Select	NP_002684.1:p.Cys208=