Canonical Allele Identifier: CA914326654
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs1568583505

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285438A>G , CM000681.2:g.40285438A>G GRCh38
NC_000019.9:g.40791345A>G , CM000681.1:g.40791345A>G GRCh37
NC_000019.8:g.45483185A>G NCBI36
NG_012038.2:g.4921T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000578123.5:c.-85+10T>C ENSP00000462022.1:n.-85+10T>C
XM_011526620.1:c.-85+10T>C XP_011524922.1:n.-85+10T>C