Canonical Allele Identifier: CA2698270941
Gene: AGT HGNC NCBI

Linked Data

dbSNP Id: rs2102795586

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230716296C>T , CM000663.2:g.230716296C>T GRCh38
NC_000001.10:g.230852042C>T , CM000663.1:g.230852042C>T GRCh37
NC_000001.9:g.228918665C>T NCBI36
NG_008836.1:g.3295G>A
NG_008836.2:g.3295G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000681269.1:c.-30-5443G>A ENSP00000505985.1:n.-30-5443G>A
NM_001382817.3:c.-30-5443G>A NP_001369746.2:n.-30-5443G>A