Canonical Allele Identifier: CA224166279
Gene: AIP HGNC NCBI

Linked Data

dbSNP Id: rs767823669
gnomAD v4: 11-67491154-T-C
MyVariant Identifiers: chr11:g.67258625T>C (hg19) chr11:g.67491154T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67491154T>C , CM000673.2:g.67491154T>C GRCh38
NC_000011.9:g.67258625T>C , CM000673.1:g.67258625T>C GRCh37
NC_000011.8:g.67015201T>C NCBI36
NG_008969.1:g.13121T>C , LRG_460:g.13121T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684657.1:c.*161T>C ENSP00000507961.1:n.*161T>C
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