Canonical Allele Identifier: CA2650970394
Gene: AGT HGNC NCBI

Linked Data

gnomAD v4: 1-230702498-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702498T>G , CM000663.2:g.230702498T>G GRCh38
NC_000001.10:g.230838244T>G , CM000663.1:g.230838244T>G GRCh37
NC_000001.9:g.228904867T>G NCBI36
NG_008836.1:g.17093A>C
NG_008836.2:g.17093A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000679738.1:c.*643A>C ENSP00000505063.1:n.*643A>C
ENST00000679802.1:c.*1533A>C ENSP00000505184.1:n.*1533A>C
ENST00000679854.1:n.6379A>C
ENST00000680041.1:c.*643A>C ENSP00000504866.1:n.*643A>C
ENST00000680783.1:c.829+7497A>C ENSP00000506329.1:n.829+7497A>C
ENST00000681347.1:n.4180A>C
ENST00000681514.1:c.*643A>C ENSP00000505963.1:n.*643A>C
ENST00000681772.1:c.*1568A>C ENSP00000505829.1:n.*1568A>C
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