Canonical Allele Identifier: CA2698267252
Gene: AGT HGNC NCBI

Linked Data

dbSNP Id: rs2102783873
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702489A>T , CM000663.2:g.230702489A>T GRCh38
NC_000001.10:g.230838235A>T , CM000663.1:g.230838235A>T GRCh37
NC_000001.9:g.228904858A>T NCBI36
NG_008836.1:g.17102T>A
NG_008836.2:g.17102T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000679738.1:c.*652T>A ENSP00000505063.1:n.*652T>A
ENST00000679802.1:c.*1542T>A ENSP00000505184.1:n.*1542T>A
ENST00000679854.1:n.6388T>A
ENST00000680041.1:c.*652T>A ENSP00000504866.1:n.*652T>A
ENST00000680783.1:c.829+7506T>A ENSP00000506329.1:n.829+7506T>A
ENST00000681347.1:n.4189T>A
ENST00000681514.1:c.*652T>A ENSP00000505963.1:n.*652T>A
ENST00000681772.1:c.*1577T>A ENSP00000505829.1:n.*1577T>A
Search 100 bp 5'
Search 100 bp 3'