Canonical Allele Identifier: CA882232862

Gene: AKT2

Linked Data

• dbSNP Id: rs1366523455
• gnomAD v3: 19-40285351-C-T
• gnomAD v4: 19-40285351-C-T
• MyVariant Identifiers: chr19:g.40791258C>T (hg19) ; chr19:g.40285351C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285351C>T , CM000681.2:g.40285351C>T	GRCh38
NC_000019.9:g.40791258C>T , CM000681.1:g.40791258C>T	GRCh37
NC_000019.8:g.45483098C>T	NCBI36
NG_012038.2:g.5008G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391844.8:c.-301G>A	ENSP00000375719.4:n.-301G>A
ENST00000392038.6:c.-255G>A	ENSP00000375892.2:n.-255G>A
ENST00000424901.5:c.-255G>A	ENSP00000399532.2:n.-255G>A
ENST00000578123.5:c.-85+97G>A	ENSP00000462022.1:n.-85+97G>A
NM_001243027.2:c.-404G>A	NP_001229956.1:n.-404G>A
NM_001243028.2:c.-311G>A	NP_001229957.1:n.-311G>A
NM_001626.5:c.-255G>A	NP_001617.1:n.-255G>A
XM_011526620.1:c.-85+97G>A	XP_011524922.1:n.-85+97G>A