Canonical Allele Identifier: CA633111015

Gene: AKT2

Linked Data

• dbSNP Id: rs1226113986
• gnomAD v2: 19-40791378-G-C
• gnomAD v3: 19-40285471-G-C
• gnomAD v4: 19-40285471-G-C
• MyVariant Identifiers: chr19:g.40791378G>C (hg19) ; chr19:g.40285471G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285471G>C , CM000681.2:g.40285471G>C	GRCh38
NC_000019.9:g.40791378G>C , CM000681.1:g.40791378G>C	GRCh37
NC_000019.8:g.45483218G>C	NCBI36
NG_012038.2:g.4888C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578123.5:c.-108C>G	ENSP00000462022.1:n.-108C>G
XM_011526620.1:c.-108C>G	XP_011524922.1:n.-108C>G