Canonical Allele Identifier: CA38862948
Gene: AGT HGNC NCBI

Linked Data

dbSNP Id: rs61751084
gnomAD v2: 1-230838144-G-T
gnomAD v3: 1-230702398-G-T
gnomAD v4: 1-230702398-G-T
MyVariant Identifiers: chr1:g.230838144G>T (hg19) chr1:g.230702398G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702398G>T , CM000663.2:g.230702398G>T GRCh38
NC_000001.10:g.230838144G>T , CM000663.1:g.230838144G>T GRCh37
NC_000001.9:g.228904767G>T NCBI36
NG_008836.1:g.17193C>A
NG_008836.2:g.17193C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000679738.1:c.*743C>A ENSP00000505063.1:n.*743C>A
ENST00000679802.1:c.*1633C>A ENSP00000505184.1:n.*1633C>A
ENST00000679854.1:n.6479C>A
ENST00000680041.1:c.*743C>A ENSP00000504866.1:n.*743C>A
ENST00000680783.1:c.829+7597C>A ENSP00000506329.1:n.829+7597C>A
ENST00000681347.1:n.4280C>A
ENST00000681514.1:c.*743C>A ENSP00000505963.1:n.*743C>A
ENST00000681772.1:c.*1668C>A ENSP00000505829.1:n.*1668C>A
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