Canonical Allele Identifier: CA308416426

Gene: AKT2

Linked Data

• dbSNP Id: rs887352984
• gnomAD v2: 19-40791386-G-C
• gnomAD v3: 19-40285479-G-C
• gnomAD v4: 19-40285479-G-C
• MyVariant Identifiers: chr19:g.40791386G>C (hg19) ; chr19:g.40285479G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285479G>C , CM000681.2:g.40285479G>C	GRCh38
NC_000019.9:g.40791386G>C , CM000681.1:g.40791386G>C	GRCh37
NC_000019.8:g.45483226G>C	NCBI36
NG_012038.2:g.4880C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000578123.5:c.-116C>G	ENSP00000462022.1:n.-116C>G
XM_011526620.1:c.-116C>G	XP_011524922.1:n.-116C>G