Canonical Allele Identifier: CA2614627910
Gene: AIP HGNC NCBI

Linked Data

gnomAD v4: 11-67491119-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67491119C>T , CM000673.2:g.67491119C>T GRCh38
NC_000011.9:g.67258590C>T , CM000673.1:g.67258590C>T GRCh37
NC_000011.8:g.67015166C>T NCBI36
NG_008969.1:g.13086C>T , LRG_460:g.13086C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684657.1:c.*126C>T ENSP00000507961.1:n.*126C>T
Search 100 bp 5'
Search 100 bp 3'