Canonical Allele Identifier: CA633110987

Gene: AKT2

Linked Data

• dbSNP Id: rs1464070270
• gnomAD v2: 19-40791289-A-C
• gnomAD v3: 19-40285382-A-C
• gnomAD v4: 19-40285382-A-C
• MyVariant Identifiers: chr19:g.40791289A>C (hg19) ; chr19:g.40285382A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285382A>C , CM000681.2:g.40285382A>C	GRCh38
NC_000019.9:g.40791289A>C , CM000681.1:g.40791289A>C	GRCh37
NC_000019.8:g.45483129A>C	NCBI36
NG_012038.2:g.4977T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000392038.6:c.-286T>G	ENSP00000375892.2:n.-286T>G
ENST00000424901.5:c.-286T>G	ENSP00000399532.2:n.-286T>G
ENST00000578123.5:c.-85+66T>G	ENSP00000462022.1:n.-85+66T>G
NM_001243027.2:c.-435T>G	NP_001229956.1:n.-435T>G
NM_001243028.2:c.-342T>G	NP_001229957.1:n.-342T>G
NM_001626.5:c.-286T>G	NP_001617.1:n.-286T>G
XM_011526620.1:c.-85+66T>G	XP_011524922.1:n.-85+66T>G