Canonical Allele Identifier: CA2611999032

Gene:

Linked Data

• gnomAD v4: 11-2444565-C-CGGGAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2444565_2444566insGGGAT , CM000673.2:g.2444565_2444566insGGGAT	GRCh38
NC_000011.9:g.2465795_2465796insGGGAT , CM000673.1:g.2465795_2465796insGGGAT	GRCh37
NC_000011.8:g.2422371_2422372insGGGAT	NCBI36
NG_008935.1:g.4575_4576insGGGAT , LRG_287:g.4575_4576insGGGAT

Transcript Alleles

HGVS	Amino-acid Change
XR_930984.1:n.5_6insATCCC