Canonical Allele Identifier: CA2059284978
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501321_102501322delinsTC , CM000674.2:g.102501321_102501322delinsTC GRCh38
NC_000012.11:g.102895099_102895100delinsTC , CM000674.1:g.102895099_102895100delinsTC GRCh37
NC_000012.10:g.101419229_101419230delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749289.1:n.1952+17433_1952+17434delinsTC