Canonical Allele Identifier: CA400640826

Gene: POLG2

Linked Data

• MyVariant Identifiers: chr17:g.62492598A>T (hg19) ; chr17:g.64496480A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.64496480A>T , CM000679.2:g.64496480A>T	GRCh38
NC_000017.10:g.62492598A>T , CM000679.1:g.62492598A>T	GRCh37
NC_000017.9:g.59923060A>T	NCBI36
NG_013029.1:g.5587T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539111.7:c.489T>A MANE Select	ENSP00000442563.2:p.Ser163Arg
ENST00000585104.2:n.460T>A
ENST00000671755.1:c.460T>A
ENST00000673460.1:c.460T>A
ENST00000539111.6:c.489T>A	ENSP00000442563.2:p.Ser163Arg
ENST00000578997.1:c.224+52T>A	ENSP00000464389.1:n.224+52T>A
ENST00000585141.5:n.540T>A
NM_007215.3:c.489T>A	NP_009146.2:p.Ser163Arg
XM_006721651.2:c.489T>A	XP_006721714.1:p.Ser163Arg
XR_243630.1:n.540T>A
XR_934357.1:n.540T>A
XR_934358.1:n.540T>A
NM_007215.4:c.489T>A MANE Select	NP_009146.2:p.Ser163Arg