Canonical Allele Identifier: CA1980172810
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67491121G= , CM000673.2:g.67491121G= GRCh38
NC_000011.9:g.67258592G= , CM000673.1:g.67258592G= GRCh37
NC_000011.8:g.67015168G= NCBI36
NG_008969.1:g.13088G= , LRG_460:g.13088G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684657.1:c.*128G= ENSP00000507961.1:n.*128G=