Canonical Allele Identifier: CA2748101306
Gene: AGT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230716372G>T , CM000663.2:g.230716372G>T GRCh38
NC_000001.10:g.230852118G>T , CM000663.1:g.230852118G>T GRCh37
NC_000001.9:g.228918741G>T NCBI36
NG_008836.1:g.3219C>A
NG_008836.2:g.3219C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000681269.1:c.-30-5519C>A ENSP00000505985.1:n.-30-5519C>A
NM_001382817.3:c.-30-5519C>A NP_001369746.2:n.-30-5519C>A
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