Canonical Allele Identifier: CA308416489

Gene: AKT2

Linked Data

• dbSNP Id: rs138126135
• gnomAD v2: 19-40791429-G-A
• gnomAD v3: 19-40285522-G-A
• gnomAD v4: 19-40285522-G-A
• MyVariant Identifiers: chr19:g.40791429G>A (hg19) ; chr19:g.40285522G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285522G>A , CM000681.2:g.40285522G>A	GRCh38
NC_000019.9:g.40791429G>A , CM000681.1:g.40791429G>A	GRCh37
NC_000019.8:g.45483269G>A	NCBI36
NG_012038.2:g.4837C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000578123.5:c.-159C>T	ENSP00000462022.1:n.-159C>T
XM_011526620.1:c.-159C>T	XP_011524922.1:n.-159C>T