Canonical Allele Identifier: CA308416466
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs1028804130

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285498A>G , CM000681.2:g.40285498A>G GRCh38
NC_000019.9:g.40791405A>G , CM000681.1:g.40791405A>G GRCh37
NC_000019.8:g.45483245A>G NCBI36
NG_012038.2:g.4861T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000578123.5:c.-135T>C ENSP00000462022.1:n.-135T>C
XM_011526620.1:c.-135T>C XP_011524922.1:n.-135T>C