Canonical Allele Identifier: CA939070179

Gene: AIP

Linked Data

• dbSNP Id: rs1865904090
• gnomAD v3: 11-67491109-GTC-G
• gnomAD v4: 11-67491109-GTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67491111_67491112del , CM000673.2:g.67491111_67491112del	GRCh38
NC_000011.9:g.67258582_67258583del , CM000673.1:g.67258582_67258583del	GRCh37
NC_000011.8:g.67015158_67015159del	NCBI36
NG_008969.1:g.13078_13079del , LRG_460:g.13078_13079del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684657.1:c.*118_*119del	ENSP00000507961.1:n.*118_*119del