Canonical Allele Identifier: CA2335910171
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs2077500314

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285500_40285502del , CM000681.2:g.40285500_40285502del GRCh38
NC_000019.9:g.40791407_40791409del , CM000681.1:g.40791407_40791409del GRCh37
NC_000019.8:g.45483247_45483249del NCBI36
NG_012038.2:g.4859_4861del

Transcript Alleles

HGVS Amino-acid Change
ENST00000578123.5:c.-137_-135del ENSP00000462022.1:n.-137_-135del
XM_011526620.1:c.-137_-135del XP_011524922.1:n.-137_-135del