Canonical Allele Identifier: CA1033291366
Gene:

Linked Data

dbSNP Id: rs1672683702

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016318_88016319insG , CM000664.2:g.88016318_88016319insG GRCh38
NC_000002.11:g.88315837_88315838insG , CM000664.1:g.88315837_88315838insG GRCh37
NC_000002.10:g.88096952_88096953insG NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.663_664insG
XR_940336.3:n.663_664insG