Canonical Allele Identifier: CA882233022

Gene: AKT2

Linked Data

• dbSNP Id: rs1421734256
• gnomAD v3: 19-40285497-G-C
• gnomAD v4: 19-40285497-G-C
• MyVariant Identifiers: chr19:g.40791404G>C (hg19) ; chr19:g.40285497G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285497G>C , CM000681.2:g.40285497G>C	GRCh38
NC_000019.9:g.40791404G>C , CM000681.1:g.40791404G>C	GRCh37
NC_000019.8:g.45483244G>C	NCBI36
NG_012038.2:g.4862C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000578123.5:c.-134C>G	ENSP00000462022.1:n.-134C>G
XM_011526620.1:c.-134C>G	XP_011524922.1:n.-134C>G