Canonical Allele Identifier: CA38862935
Gene: AGT HGNC NCBI

Linked Data

dbSNP Id: rs1027413638
gnomAD v2: 1-230838142-A-G
gnomAD v3: 1-230702396-A-G
gnomAD v4: 1-230702396-A-G
MyVariant Identifiers: chr1:g.230838142A>G (hg19) chr1:g.230702396A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702396A>G , CM000663.2:g.230702396A>G GRCh38
NC_000001.10:g.230838142A>G , CM000663.1:g.230838142A>G GRCh37
NC_000001.9:g.228904765A>G NCBI36
NG_008836.1:g.17195T>C
NG_008836.2:g.17195T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000679738.1:c.*745T>C ENSP00000505063.1:n.*745T>C
ENST00000679802.1:c.*1635T>C ENSP00000505184.1:n.*1635T>C
ENST00000679854.1:n.6481T>C
ENST00000680041.1:c.*745T>C ENSP00000504866.1:n.*745T>C
ENST00000680783.1:c.829+7599T>C ENSP00000506329.1:n.829+7599T>C
ENST00000681347.1:n.4282T>C
ENST00000681514.1:c.*745T>C ENSP00000505963.1:n.*745T>C
ENST00000681772.1:c.*1670T>C ENSP00000505829.1:n.*1670T>C
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