Canonical Allele Identifier: CA2650970372
Gene: AGT HGNC NCBI

Linked Data

gnomAD v4: 1-230702435-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702435C>T , CM000663.2:g.230702435C>T GRCh38
NC_000001.10:g.230838181C>T , CM000663.1:g.230838181C>T GRCh37
NC_000001.9:g.228904804C>T NCBI36
NG_008836.1:g.17156G>A
NG_008836.2:g.17156G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000679738.1:c.*706G>A ENSP00000505063.1:n.*706G>A
ENST00000679802.1:c.*1596G>A ENSP00000505184.1:n.*1596G>A
ENST00000679854.1:n.6442G>A
ENST00000680041.1:c.*706G>A ENSP00000504866.1:n.*706G>A
ENST00000680783.1:c.829+7560G>A ENSP00000506329.1:n.829+7560G>A
ENST00000681347.1:n.4243G>A
ENST00000681514.1:c.*706G>A ENSP00000505963.1:n.*706G>A
ENST00000681772.1:c.*1631G>A ENSP00000505829.1:n.*1631G>A
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