Canonical Allele Identifier: CA2735908170
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs1464070270

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285382A>T , CM000681.2:g.40285382A>T GRCh38
NC_000019.9:g.40791289A>T , CM000681.1:g.40791289A>T GRCh37
NC_000019.8:g.45483129A>T NCBI36
NG_012038.2:g.4977T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000392038.6:c.-286T>A ENSP00000375892.2:n.-286T>A
ENST00000424901.5:c.-286T>A ENSP00000399532.2:n.-286T>A
ENST00000578123.5:c.-85+66T>A ENSP00000462022.1:n.-85+66T>A
NM_001243027.2:c.-435T>A NP_001229956.1:n.-435T>A
NM_001243028.2:c.-342T>A NP_001229957.1:n.-342T>A
NM_001626.5:c.-286T>A NP_001617.1:n.-286T>A
XM_011526620.1:c.-85+66T>A XP_011524922.1:n.-85+66T>A