Canonical Allele Identifier: CA633111169

Gene: AKT2

Linked Data

• dbSNP Id: rs1174252952
• gnomAD v2: 19-40791433-C-CT
• MyVariant Identifiers: chr19:g.40791433_40791434insT (hg19) ; chr19:g.40285526_40285527insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285527dup , CM000681.2:g.40285527dup	GRCh38
NC_000019.9:g.40791434dup , CM000681.1:g.40791434dup	GRCh37
NC_000019.8:g.45483274dup	NCBI36
NG_012038.2:g.4832dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000578123.5:c.-164dup	ENSP00000462022.1:n.-164dup
XM_011526620.1:c.-164dup	XP_011524922.1:n.-164dup