Canonical Allele Identifier: CA1014802030
Gene:

Linked Data

dbSNP Id: rs2087099916

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2674223_2674224insAAG , CM000682.2:g.2674223_2674224insAAG GRCh38
NC_000020.10:g.2654869_2654870insAAG , CM000682.1:g.2654869_2654870insAAG GRCh37
NC_000020.9:g.2602869_2602870insAAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937210.1:n.675-3784_675-3783insCTT
XR_937211.1:n.674-3641_674-3640insCTT
XR_937210.2:n.668-3784_668-3783insCTT
XR_937211.2:n.666-3641_666-3640insCTT