Canonical Allele Identifier: CA2650970399
Gene: AGT HGNC NCBI

Linked Data

gnomAD v4: 1-230702502-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702502G>T , CM000663.2:g.230702502G>T GRCh38
NC_000001.10:g.230838248G>T , CM000663.1:g.230838248G>T GRCh37
NC_000001.9:g.228904871G>T NCBI36
NG_008836.1:g.17089C>A
NG_008836.2:g.17089C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000679738.1:c.*639C>A ENSP00000505063.1:n.*639C>A
ENST00000679802.1:c.*1529C>A ENSP00000505184.1:n.*1529C>A
ENST00000679854.1:n.6375C>A
ENST00000680041.1:c.*639C>A ENSP00000504866.1:n.*639C>A
ENST00000680783.1:c.829+7493C>A ENSP00000506329.1:n.829+7493C>A
ENST00000681347.1:n.4176C>A
ENST00000681514.1:c.*639C>A ENSP00000505963.1:n.*639C>A
ENST00000681772.1:c.*1564C>A ENSP00000505829.1:n.*1564C>A
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