Canonical Allele Identifier: CA2614617618
Gene: AIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67482962del , CM000673.2:g.67482962del GRCh38
NC_000011.9:g.67250433del , CM000673.1:g.67250433del GRCh37
NC_000011.8:g.67007009del NCBI36
NG_008969.1:g.4929del , LRG_460:g.4929del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-197del ENSP00000507935.1:n.-197del
XM_024448761.1:c.-197del XP_024304529.1:n.-197del