Canonical Allele Identifier: CA224166264
Gene: AIP HGNC NCBI

Linked Data

dbSNP Id: rs1042658640
gnomAD v2: 11-67258617-A-T
gnomAD v3: 11-67491146-A-T
gnomAD v4: 11-67491146-A-T
MyVariant Identifiers: chr11:g.67258617A>T (hg19) chr11:g.67491146A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67491146A>T , CM000673.2:g.67491146A>T GRCh38
NC_000011.9:g.67258617A>T , CM000673.1:g.67258617A>T GRCh37
NC_000011.8:g.67015193A>T NCBI36
NG_008969.1:g.13113A>T , LRG_460:g.13113A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684657.1:c.*153A>T ENSP00000507961.1:n.*153A>T
Search 100 bp 5'
Search 100 bp 3'