Canonical Allele Identifier: CA2270396455

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.64477929C= , CM000679.2:g.64477929C= GRCh38
NC_000017.10:g.62474046C= , CM000679.1:g.62474046C= GRCh37
NC_000017.9:g.59904508C= NCBI36
NG_013029.1:g.24139G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000539111.7:c.1352G= (POLG2) MANE Select ENSP00000442563.2:p.Gly451=
ENST00000585104.2:n.1524G= (POLG2)
ENST00000671755.1:c.1440G= (POLG2)
ENST00000673460.1:c.3470G= (POLG2)
ENST00000539111.6:c.1352G= (POLG2) ENSP00000442563.2:p.Gly451=
ENST00000581355.1:c.510G= (POLG2) ENSP00000462071.1:n.510G=
NM_007215.3:c.1352G= (POLG2) NP_009146.2:p.Gly451=
XM_011524627.1:c.*29-1438C= (MILR1) XP_011522929.1:n.*29-1438C=
XR_243630.1:n.1604G= (POLG2)
XR_934357.1:n.3167G= (POLG2)
XM_024450706.1:c.*28+10284C= (MILR1) XP_024306474.1:n.*28+10284C=
XM_024450708.1:c.*28+10284C= (MILR1) XP_024306476.1:n.*28+10284C=
XM_024450709.1:c.*29-1438C= (MILR1) XP_024306477.1:n.*29-1438C=
XR_002957989.1:n.1207+10284C= (MILR1)
XR_002957990.1:n.1207+10284C= (MILR1)
NM_007215.4:c.1352G= (POLG2) MANE Select NP_009146.2:p.Gly451=