Canonical Allele Identifier: CA38875400
Gene: AGT HGNC NCBI

Linked Data

dbSNP Id: rs903032326

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230714127G>A , CM000663.2:g.230714127G>A GRCh38
NC_000001.10:g.230849873G>A , CM000663.1:g.230849873G>A GRCh37
NC_000001.9:g.228916496G>A NCBI36
NG_008836.1:g.5464C>T
NG_008836.2:g.5464C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000679684.1:c.-72C>T ENSP00000505981.1:n.-72C>T
ENST00000679738.1:c.-72C>T ENSP00000505063.1:n.-72C>T
ENST00000679802.1:c.-72C>T ENSP00000505184.1:n.-72C>T
ENST00000679854.1:n.440C>T
ENST00000679957.1:c.-72C>T ENSP00000506646.1:n.-72C>T
ENST00000680041.1:c.-197C>T ENSP00000504866.1:n.-197C>T
ENST00000680783.1:c.-72C>T ENSP00000506329.1:n.-72C>T
ENST00000681269.1:c.-30-3274C>T ENSP00000505985.1:n.-30-3274C>T
ENST00000681347.1:n.440C>T
ENST00000681772.1:c.-72C>T ENSP00000505829.1:n.-72C>T
ENST00000366667.4:c.-45C>T ENSP00000355627.4:n.-45C>T
NM_000029.3:c.-45C>T NP_000020.1:n.-45C>T
NM_001382817.3:c.-30-3274C>T NP_001369746.2:n.-30-3274C>T