Canonical Allele Identifier: CA2335910070
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs1319794627

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285378G>T , CM000681.2:g.40285378G>T GRCh38
NC_000019.9:g.40791285G>T , CM000681.1:g.40791285G>T GRCh37
NC_000019.8:g.45483125G>T NCBI36
NG_012038.2:g.4981C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000392038.6:c.-282C>A ENSP00000375892.2:n.-282C>A
ENST00000424901.5:c.-282C>A ENSP00000399532.2:n.-282C>A
ENST00000578123.5:c.-85+70C>A ENSP00000462022.1:n.-85+70C>A
NM_001243027.2:c.-431C>A NP_001229956.1:n.-431C>A
NM_001243028.2:c.-338C>A NP_001229957.1:n.-338C>A
NM_001626.5:c.-282C>A NP_001617.1:n.-282C>A
XM_011526620.1:c.-85+70C>A XP_011524922.1:n.-85+70C>A