Canonical Allele Identifier: CA308416476
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs1011405629

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285504A>C , CM000681.2:g.40285504A>C GRCh38
NC_000019.9:g.40791411A>C , CM000681.1:g.40791411A>C GRCh37
NC_000019.8:g.45483251A>C NCBI36
NG_012038.2:g.4855T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000578123.5:c.-141T>G ENSP00000462022.1:n.-141T>G
XM_011526620.1:c.-141T>G XP_011524922.1:n.-141T>G