Canonical Allele Identifier: CA1691656445

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17957850_17957851delinsCT , CM000669.2:g.17957850_17957851delinsCT	GRCh38
NC_000007.13:g.17997473_17997474delinsCT , CM000669.1:g.17997473_17997474delinsCT	GRCh37
NC_000007.12:g.17963998_17963999delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_927078.1:n.271-820_271-819delinsCT