Canonical Allele Identifier: CA985496147

Linked Data

dbSNP Id: rs2038151853

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.64496407del , CM000679.2:g.64496407del GRCh38
NC_000017.10:g.62492525del , CM000679.1:g.62492525del GRCh37
NC_000017.9:g.59922987del NCBI36
NG_013029.1:g.5661del

Transcript Alleles

HGVS Amino-acid Change
ENST00000539111.7:c.562+1del (POLG2)
ENST00000585104.2:n.533+1del (POLG2)
ENST00000671755.1:c.533+1del (POLG2)
ENST00000673460.1:c.533+1del (POLG2)
ENST00000539111.6:c.562+1del (POLG2)
ENST00000578997.1:c.224+126del (POLG2) ENSP00000464389.1:n.224+126del
ENST00000585141.5:n.613+1del (POLG2)
NM_007215.3:c.562+1del (POLG2)
XM_006721651.2:c.562+1del (POLG2)
XR_243630.1:n.613+1del (POLG2)
XR_934357.1:n.613+1del (POLG2)
XR_934358.1:n.613+1del (POLG2)
XM_024450708.1:c.*115del (MILR1) XP_024306476.1:n.*115del
XR_002957990.1:n.1357del (MILR1)
NM_007215.4:c.562+1del (POLG2)