Canonical Allele Identifier: CA1226669969
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230716353T= , CM000663.2:g.230716353T= GRCh38
NC_000001.10:g.230852099T= , CM000663.1:g.230852099T= GRCh37
NC_000001.9:g.228918722T= NCBI36
NG_008836.1:g.3238A=
NG_008836.2:g.3238A=

Transcript Alleles

HGVS Amino-acid change
ENST00000681269.1:c.-30-5500A= ENSP00000505985.1:n.-30-5500A=
NM_001382817.3:c.-30-5500A= NP_001369746.2:n.-30-5500A=