Canonical Allele Identifier: CA995878757
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs1260940377
gnomAD v3: 19-40285389-C-T
gnomAD v4: 19-40285389-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285389C>T , CM000681.2:g.40285389C>T GRCh38
NC_000019.9:g.40791296C>T , CM000681.1:g.40791296C>T GRCh37
NC_000019.8:g.45483136C>T NCBI36
NG_012038.2:g.4970G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000392038.6:c.-293G>A ENSP00000375892.2:n.-293G>A
ENST00000424901.5:c.-293G>A ENSP00000399532.2:n.-293G>A
ENST00000578123.5:c.-85+59G>A ENSP00000462022.1:n.-85+59G>A
NM_001243027.2:c.-442G>A NP_001229956.1:n.-442G>A
NM_001243028.2:c.-349G>A NP_001229957.1:n.-349G>A
NM_001626.5:c.-293G>A NP_001617.1:n.-293G>A
XM_011526620.1:c.-85+59G>A XP_011524922.1:n.-85+59G>A
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