Canonical Allele Identifier: CA1980172826
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67491146A= , CM000673.2:g.67491146A= GRCh38
NC_000011.9:g.67258617A= , CM000673.1:g.67258617A= GRCh37
NC_000011.8:g.67015193A= NCBI36
NG_008969.1:g.13113A= , LRG_460:g.13113A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684657.1:c.*153A= ENSP00000507961.1:n.*153A=