Canonical Allele Identifier: CA2269954670
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63506395_63506396delinsCG , CM000679.2:g.63506395_63506396delinsCG GRCh38
NC_000017.10:g.61583756_61583757delinsCG , CM000679.1:g.61583756_61583757delinsCG GRCh37
NC_000017.9:g.58937488_58937489delinsCG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577647.2:c.1970-661_1970-660delinsCG ENSP00000464149.1:n.1970-661_1970-660delinsCG