Allele Registry

WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.

Canonical Allele Identifier: CA308416366

Gene: AKT2 HGNC NCBI

Linked Data

dbSNP Id: rs563324770

gnomAD v3: 19-40285452-A-G

gnomAD v4: 19-40285452-A-G

MyVariant Identifiers: chr19:g.40791359A>G (hg19) chr19:g.40285452A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40285452A>G , CM000681.2:g.40285452A>G	GRCh38
NC_000019.9:g.40791359A>G , CM000681.1:g.40791359A>G	GRCh37
NC_000019.8:g.45483199A>G	NCBI36
NG_012038.2:g.4907T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000578123.5:c.-89T>C	ENSP00000462022.1:n.-89T>C
XM_011526620.1:c.-89T>C	XP_011524922.1:n.-89T>C

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