Canonical Allele Identifier: CA38877142
Gene: AGT HGNC NCBI

Linked Data

dbSNP Id: rs557314499
gnomAD v3: 1-230716366-T-A
gnomAD v4: 1-230716366-T-A
MyVariant Identifiers: chr1:g.230852112T>A (hg19) chr1:g.230716366T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230716366T>A , CM000663.2:g.230716366T>A GRCh38
NC_000001.10:g.230852112T>A , CM000663.1:g.230852112T>A GRCh37
NC_000001.9:g.228918735T>A NCBI36
NG_008836.1:g.3225A>T
NG_008836.2:g.3225A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000681269.1:c.-30-5513A>T ENSP00000505985.1:n.-30-5513A>T
NM_001382817.3:c.-30-5513A>T NP_001369746.2:n.-30-5513A>T
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