Canonical Allele Identifier: CA2650970367

Gene: AGT

Linked Data

• gnomAD v4: 1-230702429-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702429G>A , CM000663.2:g.230702429G>A	GRCh38
NC_000001.10:g.230838175G>A , CM000663.1:g.230838175G>A	GRCh37
NC_000001.9:g.228904798G>A	NCBI36
NG_008836.1:g.17162C>T
NG_008836.2:g.17162C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000679738.1:c.*712C>T	ENSP00000505063.1:n.*712C>T
ENST00000679802.1:c.*1602C>T	ENSP00000505184.1:n.*1602C>T
ENST00000679854.1:n.6448C>T
ENST00000680041.1:c.*712C>T	ENSP00000504866.1:n.*712C>T
ENST00000680783.1:c.829+7566C>T	ENSP00000506329.1:n.829+7566C>T
ENST00000681347.1:n.4249C>T
ENST00000681514.1:c.*712C>T	ENSP00000505963.1:n.*712C>T
ENST00000681772.1:c.*1637C>T	ENSP00000505829.1:n.*1637C>T