Canonical Allele Identifier: CA308416376
Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs992715778
gnomAD v4: 19-40285468-T-A
MyVariant Identifiers: chr19:g.40791375T>A (hg19) chr19:g.40285468T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40285468T>A , CM000681.2:g.40285468T>A GRCh38
NC_000019.9:g.40791375T>A , CM000681.1:g.40791375T>A GRCh37
NC_000019.8:g.45483215T>A NCBI36
NG_012038.2:g.4891A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000578123.5:c.-105A>T ENSP00000462022.1:n.-105A>T
XM_011526620.1:c.-105A>T XP_011524922.1:n.-105A>T
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