Canonical Allele Identifier: CA633111014
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs1327837509
gnomAD v2: 19-40791374-CTG-C
gnomAD v3: 19-40285467-CTG-C
gnomAD v4: 19-40285467-CTG-C
MyVariant Identifiers: chr19:g.40791375_40791376del (hg19) chr19:g.40285468_40285469del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285468_40285469del , CM000681.2:g.40285468_40285469del GRCh38
NC_000019.9:g.40791375_40791376del , CM000681.1:g.40791375_40791376del GRCh37
NC_000019.8:g.45483215_45483216del NCBI36
NG_012038.2:g.4890_4891del

Transcript Alleles

HGVS Amino-acid Change
ENST00000578123.5:c.-106_-105del ENSP00000462022.1:n.-106_-105del
XM_011526620.1:c.-106_-105del XP_011524922.1:n.-106_-105del
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