Canonical Allele Identifier: CA2335910088
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs1217423582

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285392C>T , CM000681.2:g.40285392C>T GRCh38
NC_000019.9:g.40791299C>T , CM000681.1:g.40791299C>T GRCh37
NC_000019.8:g.45483139C>T NCBI36
NG_012038.2:g.4967G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000392038.6:c.-296G>A ENSP00000375892.2:n.-296G>A
ENST00000424901.5:c.-296G>A ENSP00000399532.2:n.-296G>A
ENST00000578123.5:c.-85+56G>A ENSP00000462022.1:n.-85+56G>A
NM_001243027.2:c.-445G>A NP_001229956.1:n.-445G>A
NM_001243028.2:c.-352G>A NP_001229957.1:n.-352G>A
NM_001626.5:c.-296G>A NP_001617.1:n.-296G>A
XM_011526620.1:c.-85+56G>A XP_011524922.1:n.-85+56G>A