Canonical Allele Identifier: CA1689218015

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.13400532_13400533delinsCT , CM000669.2:g.13400532_13400533delinsCT	GRCh38
NC_000007.13:g.13440157_13440158delinsCT , CM000669.1:g.13440157_13440158delinsCT	GRCh37
NC_000007.12:g.13406682_13406683delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001745097.1:n.147+90209_147+90210delinsCT