Canonical Allele Identifier: CA1226669959
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230716330A= , CM000663.2:g.230716330A= GRCh38
NC_000001.10:g.230852076A= , CM000663.1:g.230852076A= GRCh37
NC_000001.9:g.228918699A= NCBI36
NG_008836.1:g.3261T=
NG_008836.2:g.3261T=

Transcript Alleles

HGVS Amino-acid change
ENST00000681269.1:c.-30-5477T= ENSP00000505985.1:n.-30-5477T=
NM_001382817.3:c.-30-5477T= NP_001369746.2:n.-30-5477T=