Canonical Allele Identifier: CA2755810836
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.34921318_34921319insA , CM000665.2:g.34921318_34921319insA GRCh38
NC_000003.11:g.34962810_34962811insA , CM000665.1:g.34962810_34962811insA GRCh37
NC_000003.10:g.34937814_34937815insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110817.1:n.207-41853_207-41852insT