Canonical Allele Identifier: CA633110986

Gene: AKT2

Linked Data

• dbSNP Id: rs1273230100
• gnomAD v2: 19-40791288-T-C
• gnomAD v3: 19-40285381-T-C
• gnomAD v4: 19-40285381-T-C
• MyVariant Identifiers: chr19:g.40791288T>C (hg19) ; chr19:g.40285381T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285381T>C , CM000681.2:g.40285381T>C	GRCh38
NC_000019.9:g.40791288T>C , CM000681.1:g.40791288T>C	GRCh37
NC_000019.8:g.45483128T>C	NCBI36
NG_012038.2:g.4978A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000392038.6:c.-285A>G	ENSP00000375892.2:n.-285A>G
ENST00000424901.5:c.-285A>G	ENSP00000399532.2:n.-285A>G
ENST00000578123.5:c.-85+67A>G	ENSP00000462022.1:n.-85+67A>G
NM_001243027.2:c.-434A>G	NP_001229956.1:n.-434A>G
NM_001243028.2:c.-341A>G	NP_001229957.1:n.-341A>G
NM_001626.5:c.-285A>G	NP_001617.1:n.-285A>G
XM_011526620.1:c.-85+67A>G	XP_011524922.1:n.-85+67A>G