Canonical Allele Identifier: CA2335910080
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs1243531247

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285386C>A , CM000681.2:g.40285386C>A GRCh38
NC_000019.9:g.40791293C>A , CM000681.1:g.40791293C>A GRCh37
NC_000019.8:g.45483133C>A NCBI36
NG_012038.2:g.4973G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000392038.6:c.-290G>T ENSP00000375892.2:n.-290G>T
ENST00000424901.5:c.-290G>T ENSP00000399532.2:n.-290G>T
ENST00000578123.5:c.-85+62G>T ENSP00000462022.1:n.-85+62G>T
NM_001243027.2:c.-439G>T NP_001229956.1:n.-439G>T
NM_001243028.2:c.-346G>T NP_001229957.1:n.-346G>T
NM_001626.5:c.-290G>T NP_001617.1:n.-290G>T
XM_011526620.1:c.-85+62G>T XP_011524922.1:n.-85+62G>T