Canonical Allele Identifier: CA633110994

Gene: AKT2

Linked Data

• dbSNP Id: rs1217423582
• gnomAD v2: 19-40791299-C-G
• gnomAD v3: 19-40285392-C-G
• gnomAD v4: 19-40285392-C-G
• MyVariant Identifiers: chr19:g.40791299C>G (hg19) ; chr19:g.40285392C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285392C>G , CM000681.2:g.40285392C>G	GRCh38
NC_000019.9:g.40791299C>G , CM000681.1:g.40791299C>G	GRCh37
NC_000019.8:g.45483139C>G	NCBI36
NG_012038.2:g.4967G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.6:c.-296G>C	ENSP00000375892.2:n.-296G>C
ENST00000424901.5:c.-296G>C	ENSP00000399532.2:n.-296G>C
ENST00000578123.5:c.-85+56G>C	ENSP00000462022.1:n.-85+56G>C
NM_001243027.2:c.-445G>C	NP_001229956.1:n.-445G>C
NM_001243028.2:c.-352G>C	NP_001229957.1:n.-352G>C
NM_001626.5:c.-296G>C	NP_001617.1:n.-296G>C
XM_011526620.1:c.-85+56G>C	XP_011524922.1:n.-85+56G>C