Canonical Allele Identifier: CA1267947568
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016351_88016353delinsGTT , CM000664.2:g.88016351_88016353delinsGTT GRCh38
NC_000002.11:g.88315870_88315872delinsGTT , CM000664.1:g.88315870_88315872delinsGTT GRCh37
NC_000002.10:g.88096985_88096987delinsGTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.696_698delinsGTT
XR_940336.3:n.696_698delinsGTT