Canonical Allele Identifier: CA15095150
Gene: AGT HGNC NCBI

Linked Data

dbSNP Id: rs2493137

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230716370T>C , CM000663.2:g.230716370T>C GRCh38
NC_000001.10:g.230852116T>C , CM000663.1:g.230852116T>C GRCh37
NC_000001.9:g.228918739T>C NCBI36
NG_008836.1:g.3221A>G
NG_008836.2:g.3221A>G

Transcript Alleles

HGVS Amino-acid change
NM_001382817.3:c.-30-5517A>G NP_001369746.2:p.=