Canonical Allele Identifier: CA995880830
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs2077499703

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285462G>A , CM000681.2:g.40285462G>A GRCh38
NC_000019.9:g.40791369G>A , CM000681.1:g.40791369G>A GRCh37
NC_000019.8:g.45483209G>A NCBI36
NG_012038.2:g.4897C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000578123.5:c.-99C>T ENSP00000462022.1:n.-99C>T
XM_011526620.1:c.-99C>T XP_011524922.1:n.-99C>T