Canonical Allele Identifier: CA501458829

Gene: POLG2 MILR1

Linked Data

• MyVariant Identifiers: chr17:g.62492562T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.64496444T>C , CM000679.2:g.64496444T>C	GRCh38
NC_000017.10:g.62492562T>C , CM000679.1:g.62492562T>C	GRCh37
NC_000017.9:g.59923024T>C	NCBI36
NG_013029.1:g.5623A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539111.7:c.525A>G (POLG2) MANE Select	ENSP00000442563.2:p.Leu175=
ENST00000585104.2:n.496A>G (POLG2)
ENST00000671755.1:c.496A>G (POLG2)
ENST00000673460.1:c.496A>G (POLG2)
ENST00000539111.6:c.525A>G (POLG2)	ENSP00000442563.2:p.Leu175=
ENST00000578997.1:c.224+88A>G (POLG2)	ENSP00000464389.1:n.224+88A>G
ENST00000585141.5:n.576A>G (POLG2)
NM_007215.3:c.525A>G (POLG2)	NP_009146.2:p.Leu175=
XM_006721651.2:c.525A>G (POLG2)	XP_006721714.1:p.Leu175=
XR_243630.1:n.576A>G (POLG2)
XR_934357.1:n.576A>G (POLG2)
XR_934358.1:n.576A>G (POLG2)
XM_024450708.1:c.*152T>C (MILR1)	XP_024306476.1:n.*152T>C
XR_002957990.1:n.1394T>C (MILR1)
NM_007215.4:c.525A>G (POLG2) MANE Select	NP_009146.2:p.Leu175=