Canonical Allele Identifier: CA308416338
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs963743698
gnomAD v2: 19-40791327-C-T
gnomAD v3: 19-40285420-C-T
gnomAD v4: 19-40285420-C-T
MyVariant Identifiers: chr19:g.40791327C>T (hg19) chr19:g.40285420C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285420C>T , CM000681.2:g.40285420C>T GRCh38
NC_000019.9:g.40791327C>T , CM000681.1:g.40791327C>T GRCh37
NC_000019.8:g.45483167C>T NCBI36
NG_012038.2:g.4939G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000578123.5:c.-85+28G>A ENSP00000462022.1:n.-85+28G>A
XM_011526620.1:c.-85+28G>A XP_011524922.1:n.-85+28G>A
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