Canonical Allele Identifier: CA2335910089
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs1412078145

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285395A>G , CM000681.2:g.40285395A>G GRCh38
NC_000019.9:g.40791302A>G , CM000681.1:g.40791302A>G GRCh37
NC_000019.8:g.45483142A>G NCBI36
NG_012038.2:g.4964T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000392038.6:c.-299T>C ENSP00000375892.2:n.-299T>C
ENST00000424901.5:c.-299T>C ENSP00000399532.2:n.-299T>C
ENST00000578123.5:c.-85+53T>C ENSP00000462022.1:n.-85+53T>C
NM_001243027.2:c.-448T>C NP_001229956.1:n.-448T>C
NM_001243028.2:c.-355T>C NP_001229957.1:n.-355T>C
NM_001626.5:c.-299T>C NP_001617.1:n.-299T>C
XM_011526620.1:c.-85+53T>C XP_011524922.1:n.-85+53T>C