Canonical Allele Identifier: CA308416471

Gene: AKT2

Linked Data

• dbSNP Id: rs528223387
• gnomAD v3: 19-40285501-A-G
• gnomAD v4: 19-40285501-A-G
• MyVariant Identifiers: chr19:g.40791408A>G (hg19) ; chr19:g.40285501A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285501A>G , CM000681.2:g.40285501A>G	GRCh38
NC_000019.9:g.40791408A>G , CM000681.1:g.40791408A>G	GRCh37
NC_000019.8:g.45483248A>G	NCBI36
NG_012038.2:g.4858T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000578123.5:c.-138T>C	ENSP00000462022.1:n.-138T>C
XM_011526620.1:c.-138T>C	XP_011524922.1:n.-138T>C