Canonical Allele Identifier: CA1980172825
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67491144T= , CM000673.2:g.67491144T= GRCh38
NC_000011.9:g.67258615T= , CM000673.1:g.67258615T= GRCh37
NC_000011.8:g.67015191T= NCBI36
NG_008969.1:g.13111T= , LRG_460:g.13111T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684657.1:c.*151T= ENSP00000507961.1:n.*151T=