Canonical Allele Identifier: CA732699360
Gene: AGT HGNC NCBI

Linked Data

dbSNP Id: rs1337141484
gnomAD v3: 1-230716333-C-T
gnomAD v4: 1-230716333-C-T
MyVariant Identifiers: chr1:g.230852079C>T (hg19) chr1:g.230716333C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230716333C>T , CM000663.2:g.230716333C>T GRCh38
NC_000001.10:g.230852079C>T , CM000663.1:g.230852079C>T GRCh37
NC_000001.9:g.228918702C>T NCBI36
NG_008836.1:g.3258G>A
NG_008836.2:g.3258G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000681269.1:c.-30-5480G>A ENSP00000505985.1:n.-30-5480G>A
NM_001382817.3:c.-30-5480G>A NP_001369746.2:n.-30-5480G>A
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