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: CA732699344

Gene: AGT HGNC NCBI

Linked Data

dbSNP Id: rs1205691225

MyVariant Identifiers: chr1:g.230852045_230852047del (hg19) chr1:g.230716299_230716301del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230716299_230716301del , CM000663.2:g.230716299_230716301del	GRCh38
NC_000001.10:g.230852045_230852047del , CM000663.1:g.230852045_230852047del	GRCh37
NC_000001.9:g.228918668_228918670del	NCBI36
NG_008836.1:g.3290_3292del
NG_008836.2:g.3290_3292del

Transcript Alleles

HGVS	Amino-acid change
ENST00000681269.1:c.-30-5448_-30-5446del	ENSP00000505985.1:n.-30-5448_-30-5446del
NM_001382817.3:c.-30-5448_-30-5446del	NP_001369746.2:n.-30-5448_-30-5446del

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