Canonical Allele Identifier: CA2650970420
Gene: AGT HGNC NCBI

Linked Data

gnomAD v4: 1-230702517-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702517A>T , CM000663.2:g.230702517A>T GRCh38
NC_000001.10:g.230838263A>T , CM000663.1:g.230838263A>T GRCh37
NC_000001.9:g.228904886A>T NCBI36
NG_008836.1:g.17074T>A
NG_008836.2:g.17074T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000679738.1:c.*624T>A ENSP00000505063.1:n.*624T>A
ENST00000679802.1:c.*1514T>A ENSP00000505184.1:n.*1514T>A
ENST00000679854.1:n.6360T>A
ENST00000680041.1:c.*624T>A ENSP00000504866.1:n.*624T>A
ENST00000680783.1:c.829+7478T>A ENSP00000506329.1:n.829+7478T>A
ENST00000681347.1:n.4161T>A
ENST00000681514.1:c.*624T>A ENSP00000505963.1:n.*624T>A
ENST00000681772.1:c.*1549T>A ENSP00000505829.1:n.*1549T>A
Search 100 bp 5'
Search 100 bp 3'