Canonical Allele Identifier: CA1980170049
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67483012T= , CM000673.2:g.67483012T= GRCh38
NC_000011.9:g.67250483T= , CM000673.1:g.67250483T= GRCh37
NC_000011.8:g.67007059T= NCBI36
NG_008969.1:g.4979T= , LRG_460:g.4979T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-147T= ENSP00000507935.1:n.-147T=
XM_024448761.1:c.-147T= XP_024304529.1:n.-147T=