Canonical Allele Identifier: CA599911480

Gene: AIP

Linked Data

• dbSNP Id: rs1414650776
• gnomAD v2: 11-67258609-G-A
• gnomAD v3: 11-67491138-G-A
• gnomAD v4: 11-67491138-G-A
• MyVariant Identifiers: chr11:g.67258609G>A (hg19) ; chr11:g.67491138G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67491138G>A , CM000673.2:g.67491138G>A	GRCh38
NC_000011.9:g.67258609G>A , CM000673.1:g.67258609G>A	GRCh37
NC_000011.8:g.67015185G>A	NCBI36
NG_008969.1:g.13105G>A , LRG_460:g.13105G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684657.1:c.*145G>A	ENSP00000507961.1:n.*145G>A