Canonical Allele Identifier: CA1980170035
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67482984C= , CM000673.2:g.67482984C= GRCh38
NC_000011.9:g.67250455C= , CM000673.1:g.67250455C= GRCh37
NC_000011.8:g.67007031C= NCBI36
NG_008969.1:g.4951C= , LRG_460:g.4951C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-175C= ENSP00000507935.1:n.-175C=
XM_024448761.1:c.-175C= XP_024304529.1:n.-175C=