Canonical Allele Identifier: CA2614628056
Gene: AIP HGNC NCBI

Linked Data

gnomAD v4: 11-67491147-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67491147C>G , CM000673.2:g.67491147C>G GRCh38
NC_000011.9:g.67258618C>G , CM000673.1:g.67258618C>G GRCh37
NC_000011.8:g.67015194C>G NCBI36
NG_008969.1:g.13114C>G , LRG_460:g.13114C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684657.1:c.*154C>G ENSP00000507961.1:n.*154C>G
Search 100 bp 5'
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