Canonical Allele Identifier: CA633110970

Gene: AKT2

Linked Data

• dbSNP Id: rs1293586348
• gnomAD v2: 19-40791264-C-A
• gnomAD v3: 19-40285357-C-A
• gnomAD v4: 19-40285357-C-A
• MyVariant Identifiers: chr19:g.40791264C>A (hg19) ; chr19:g.40791264_40791265delinsAG (hg19) ; chr19:g.40285357C>A (hg38) ; chr19:g.40285357_40285358delinsAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285357C>A , CM000681.2:g.40285357C>A	GRCh38
NC_000019.9:g.40791264C>A , CM000681.1:g.40791264C>A	GRCh37
NC_000019.8:g.45483104C>A	NCBI36
NG_012038.2:g.5002G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391844.8:c.-307G>T	ENSP00000375719.4:n.-307G>T
ENST00000392038.6:c.-261G>T	ENSP00000375892.2:n.-261G>T
ENST00000424901.5:c.-261G>T	ENSP00000399532.2:n.-261G>T
ENST00000578123.5:c.-85+91G>T	ENSP00000462022.1:n.-85+91G>T
NM_001243027.2:c.-410G>T	NP_001229956.1:n.-410G>T
NM_001243028.2:c.-317G>T	NP_001229957.1:n.-317G>T
NM_001626.5:c.-261G>T	NP_001617.1:n.-261G>T
XM_011526620.1:c.-85+91G>T	XP_011524922.1:n.-85+91G>T