Canonical Allele Identifier: CA1980170017
Gene: AIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67482957G= , CM000673.2:g.67482957G= GRCh38
NC_000011.9:g.67250428G= , CM000673.1:g.67250428G= GRCh37
NC_000011.8:g.67007004G= NCBI36
NG_008969.1:g.4924G= , LRG_460:g.4924G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-202G= ENSP00000507935.1:n.-202G=
XM_024448761.1:c.-202G= XP_024304529.1:n.-202G=