Canonical Allele Identifier: CA1980172814
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67491124C= , CM000673.2:g.67491124C= GRCh38
NC_000011.9:g.67258595C= , CM000673.1:g.67258595C= GRCh37
NC_000011.8:g.67015171C= NCBI36
NG_008969.1:g.13091C= , LRG_460:g.13091C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684657.1:c.*131C= ENSP00000507961.1:n.*131C=