Canonical Allele Identifier: CA501458836

Gene: POLG2 MILR1

Linked Data

• MyVariant Identifiers: chr17:g.62492574A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.64496456A>T , CM000679.2:g.64496456A>T	GRCh38
NC_000017.10:g.62492574A>T , CM000679.1:g.62492574A>T	GRCh37
NC_000017.9:g.59923036A>T	NCBI36
NG_013029.1:g.5611T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539111.7:c.513T>A (POLG2) MANE Select	ENSP00000442563.2:p.Leu171=
ENST00000585104.2:n.484T>A (POLG2)
ENST00000671755.1:c.484T>A (POLG2)
ENST00000673460.1:c.484T>A (POLG2)
ENST00000539111.6:c.513T>A (POLG2)	ENSP00000442563.2:p.Leu171=
ENST00000578997.1:c.224+76T>A (POLG2)	ENSP00000464389.1:n.224+76T>A
ENST00000585141.5:n.564T>A (POLG2)
NM_007215.3:c.513T>A (POLG2)	NP_009146.2:p.Leu171=
XM_006721651.2:c.513T>A (POLG2)	XP_006721714.1:p.Leu171=
XR_243630.1:n.564T>A (POLG2)
XR_934357.1:n.564T>A (POLG2)
XR_934358.1:n.564T>A (POLG2)
XM_024450708.1:c.*164A>T (MILR1)	XP_024306476.1:n.*164A>T
XR_002957990.1:n.1406A>T (MILR1)
NM_007215.4:c.513T>A (POLG2) MANE Select	NP_009146.2:p.Leu171=