Canonical Allele Identifier: CA2269954687
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63506437_63506439delinsCCT , CM000679.2:g.63506437_63506439delinsCCT GRCh38
NC_000017.10:g.61583798_61583800delinsCCT , CM000679.1:g.61583798_61583800delinsCCT GRCh37
NC_000017.9:g.58937530_58937532delinsCCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577647.2:c.1970-619_1970-617delinsCCT ENSP00000464149.1:n.1970-619_1970-617delinsCCT