Canonical Allele Identifier: CA679494838
Gene: AIP HGNC NCBI

Linked Data

dbSNP Id: rs1202378488
gnomAD v3: 11-67491125-C-T
gnomAD v4: 11-67491125-C-T
MyVariant Identifiers: chr11:g.67258596C>T (hg19) chr11:g.67491125C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67491125C>T , CM000673.2:g.67491125C>T GRCh38
NC_000011.9:g.67258596C>T , CM000673.1:g.67258596C>T GRCh37
NC_000011.8:g.67015172C>T NCBI36
NG_008969.1:g.13092C>T , LRG_460:g.13092C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684657.1:c.*132C>T ENSP00000507961.1:n.*132C>T
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