Canonical Allele Identifier: CA308416485

Gene: AKT2

Linked Data

• dbSNP Id: rs945642734
• gnomAD v4: 19-40285518-C-T
• MyVariant Identifiers: chr19:g.40791425C>T (hg19) ; chr19:g.40285518C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285518C>T , CM000681.2:g.40285518C>T	GRCh38
NC_000019.9:g.40791425C>T , CM000681.1:g.40791425C>T	GRCh37
NC_000019.8:g.45483265C>T	NCBI36
NG_012038.2:g.4841G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000578123.5:c.-155G>A	ENSP00000462022.1:n.-155G>A
XM_011526620.1:c.-155G>A	XP_011524922.1:n.-155G>A