Canonical Allele Identifier: CA308416365
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs563324770

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285452A>C , CM000681.2:g.40285452A>C GRCh38
NC_000019.9:g.40791359A>C , CM000681.1:g.40791359A>C GRCh37
NC_000019.8:g.45483199A>C NCBI36
NG_012038.2:g.4907T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000578123.5:c.-89T>G ENSP00000462022.1:n.-89T>G
XM_011526620.1:c.-89T>G XP_011524922.1:n.-89T>G