Canonical Allele Identifier: CA920480110
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.624389_624390insG , CM000686.2:g.624389_624390insG GRCh38
NC_000024.9:g.535124_535125insG , CM000686.1:g.535124_535125insG GRCh37
NC_000024.8:g.505124_505125insG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000711143.1:c.-646_-645insG ENSP00000518641.1:n.-646_-645insG
ENST00000711145.1:c.-646_-645insG ENSP00000518642.1:n.-646_-645insG