Canonical Allele Identifier: CA308416318

Gene: AKT2

Linked Data

• dbSNP Id: rs953306684
• gnomAD v2: 19-40791295-C-T
• gnomAD v3: 19-40285388-C-T
• gnomAD v4: 19-40285388-C-T
• MyVariant Identifiers: chr19:g.40791295C>T (hg19) ; chr19:g.40285388C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285388C>T , CM000681.2:g.40285388C>T	GRCh38
NC_000019.9:g.40791295C>T , CM000681.1:g.40791295C>T	GRCh37
NC_000019.8:g.45483135C>T	NCBI36
NG_012038.2:g.4971G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000392038.6:c.-292G>A	ENSP00000375892.2:n.-292G>A
ENST00000424901.5:c.-292G>A	ENSP00000399532.2:n.-292G>A
ENST00000578123.5:c.-85+60G>A	ENSP00000462022.1:n.-85+60G>A
NM_001243027.2:c.-441G>A	NP_001229956.1:n.-441G>A
NM_001243028.2:c.-348G>A	NP_001229957.1:n.-348G>A
NM_001626.5:c.-292G>A	NP_001617.1:n.-292G>A
XM_011526620.1:c.-85+60G>A	XP_011524922.1:n.-85+60G>A