Canonical Allele Identifier: CA2581703155
Gene: AGT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230716370T>G , CM000663.2:g.230716370T>G GRCh38
NC_000001.10:g.230852116T>G , CM000663.1:g.230852116T>G GRCh37
NC_000001.9:g.228918739T>G NCBI36
NG_008836.1:g.3221A>C
NG_008836.2:g.3221A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000681269.1:c.-30-5517A>C ENSP00000505985.1:n.-30-5517A>C
NM_001382817.3:c.-30-5517A>C NP_001369746.2:n.-30-5517A>C
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