Canonical Allele Identifier: CA633110998
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs1354241883

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285401_40285412del , CM000681.2:g.40285401_40285412del GRCh38
NC_000019.9:g.40791308_40791319del , CM000681.1:g.40791308_40791319del GRCh37
NC_000019.8:g.45483148_45483159del NCBI36
NG_012038.2:g.4947_4958del

Transcript Alleles

HGVS Amino-acid change
ENST00000578123.5:c.-85+36_-85+47del ENSP00000462022.1:n.-85+36_-85+47del
XM_011526620.1:c.-85+36_-85+47del XP_011524922.1:n.-85+36_-85+47del