Canonical Allele Identifier: CA633110971
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs1405129198
gnomAD v2: 19-40791264-CG-C
gnomAD v3: 19-40285357-CG-C
gnomAD v4: 19-40285357-CG-C
MyVariant Identifiers: chr19:g.40791265del (hg19) chr19:g.40285358del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285358del , CM000681.2:g.40285358del GRCh38
NC_000019.9:g.40791265del , CM000681.1:g.40791265del GRCh37
NC_000019.8:g.45483105del NCBI36
NG_012038.2:g.5001del

Transcript Alleles

HGVS Amino-acid Change
ENST00000391844.8:c.-308del ENSP00000375719.4:n.-308del
ENST00000392038.6:c.-262del ENSP00000375892.2:n.-262del
ENST00000424901.5:c.-262del ENSP00000399532.2:n.-262del
ENST00000578123.5:c.-85+90del ENSP00000462022.1:n.-85+90del
NM_001243027.2:c.-411del NP_001229956.1:n.-411del
NM_001243028.2:c.-318del NP_001229957.1:n.-318del
NM_001626.5:c.-262del NP_001617.1:n.-262del
XM_011526620.1:c.-85+90del XP_011524922.1:n.-85+90del
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