Canonical Allele Identifier: CA882233031
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs1194616755
MyVariant Identifiers: chr19:g.40791427del (hg19) chr19:g.40285520del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285522del , CM000681.2:g.40285522del GRCh38
NC_000019.9:g.40791429del , CM000681.1:g.40791429del GRCh37
NC_000019.8:g.45483269del NCBI36
NG_012038.2:g.4839del

Transcript Alleles

HGVS Amino-acid Change
ENST00000578123.5:c.-157del ENSP00000462022.1:n.-157del
XM_011526620.1:c.-157del XP_011524922.1:n.-157del
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