Canonical Allele Identifier: CA1226669982
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230716384A= , CM000663.2:g.230716384A= GRCh38
NC_000001.10:g.230852130A= , CM000663.1:g.230852130A= GRCh37
NC_000001.9:g.228918753A= NCBI36
NG_008836.1:g.3207T=
NG_008836.2:g.3207T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000681269.1:c.-30-5531T= ENSP00000505985.1:n.-30-5531T=
NM_001382817.3:c.-30-5531T= NP_001369746.2:n.-30-5531T=