Canonical Allele Identifier: CA1149397038
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2036587_2036591delinsGCTGT , CM000663.2:g.2036587_2036591delinsGCTGT GRCh38
NC_000001.10:g.1968026_1968030delinsGCTGT , CM000663.1:g.1968026_1968030delinsGCTGT GRCh37
NC_000001.9:g.1957886_1957890delinsGCTGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_946823.1:n.617_621delinsACAGC
XR_001737845.2:n.620_624delinsACAGC
XR_946823.3:n.620_624delinsACAGC