Canonical Allele Identifier: CA633110996

Gene: AKT2

Linked Data

• dbSNP Id: rs1412078145
• gnomAD v2: 19-40791302-A-C
• gnomAD v3: 19-40285395-A-C
• gnomAD v4: 19-40285395-A-C
• MyVariant Identifiers: chr19:g.40791302A>C (hg19) ; chr19:g.40285395A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285395A>C , CM000681.2:g.40285395A>C	GRCh38
NC_000019.9:g.40791302A>C , CM000681.1:g.40791302A>C	GRCh37
NC_000019.8:g.45483142A>C	NCBI36
NG_012038.2:g.4964T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392038.6:c.-299T>G	ENSP00000375892.2:n.-299T>G
ENST00000424901.5:c.-299T>G	ENSP00000399532.2:n.-299T>G
ENST00000578123.5:c.-85+53T>G	ENSP00000462022.1:n.-85+53T>G
NM_001243027.2:c.-448T>G	NP_001229956.1:n.-448T>G
NM_001243028.2:c.-355T>G	NP_001229957.1:n.-355T>G
NM_001626.5:c.-299T>G	NP_001617.1:n.-299T>G
XM_011526620.1:c.-85+53T>G	XP_011524922.1:n.-85+53T>G