Canonical Allele Identifier: CA1226669972
Gene: AGT HGNC NCBI

Linked Data

dbSNP Id: rs1663737045

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230716355T>A , CM000663.2:g.230716355T>A GRCh38
NC_000001.10:g.230852101T>A , CM000663.1:g.230852101T>A GRCh37
NC_000001.9:g.228918724T>A NCBI36
NG_008836.1:g.3236A>T
NG_008836.2:g.3236A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000681269.1:c.-30-5502A>T ENSP00000505985.1:n.-30-5502A>T
NM_001382817.3:c.-30-5502A>T NP_001369746.2:n.-30-5502A>T