Canonical Allele Identifier: CA2614617612

Gene: AIP

Linked Data

• gnomAD v4: 11-67482957-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67482962dup , CM000673.2:g.67482962dup	GRCh38
NC_000011.9:g.67250433dup , CM000673.1:g.67250433dup	GRCh37
NC_000011.8:g.67007009dup	NCBI36
NG_008969.1:g.4929dup , LRG_460:g.4929dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682699.1:c.-197dup	ENSP00000507935.1:n.-197dup
XM_024448761.1:c.-197dup	XP_024304529.1:n.-197dup