Canonical Allele Identifier: CA2614617957
Gene: AIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.67483026C>A , CM000673.2:g.67483026C>A GRCh38
NC_000011.9:g.67250497C>A , CM000673.1:g.67250497C>A GRCh37
NC_000011.8:g.67007073C>A NCBI36
NG_008969.1:g.4993C>A , LRG_460:g.4993C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682699.1:c.-133C>A ENSP00000507935.1:n.-133C>A
ENST00000279146.8:c.-133C>A MANE Select ENSP00000279146.3:n.-133C>A
XM_024448761.1:c.-133C>A XP_024304529.1:n.-133C>A
NM_003977.4:c.-133C>A MANE Select NP_003968.3:n.-133C>A
NM_001302960.2:c.-133C>A NP_001289889.1:n.-133C>A