Canonical Allele Identifier: CA1013241771
Gene: AGT HGNC NCBI

Linked Data

dbSNP Id: rs1663736980

Genomic Alleles

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

Transcript Alleles

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