Canonical Allele Identifier: CA2792512398
Gene: AIP HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67491123T>C , CM000673.2:g.67491123T>C GRCh38
NC_000011.9:g.67258594T>C , CM000673.1:g.67258594T>C GRCh37
NC_000011.8:g.67015170T>C NCBI36
NG_008969.1:g.13090T>C , LRG_460:g.13090T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684657.1:c.*130T>C ENSP00000507961.1:n.*130T>C
Search 100 bp 5'
Search 100 bp 3'