Canonical Allele Identifier: CA38862930

Gene: AGT

Linked Data

• dbSNP Id: rs34433365
• MyVariant Identifiers: chr1:g.230838139_230838140insA (hg19) ; chr1:g.230702393_230702394insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702396dup , CM000663.2:g.230702396dup	GRCh38
NC_000001.10:g.230838142dup , CM000663.1:g.230838142dup	GRCh37
NC_000001.9:g.228904765dup	NCBI36
NG_008836.1:g.17197dup
NG_008836.2:g.17197dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000679738.1:c.*747dup	ENSP00000505063.1:n.*747dup
ENST00000679802.1:c.*1637dup	ENSP00000505184.1:n.*1637dup
ENST00000679854.1:n.6483dup
ENST00000680041.1:c.*747dup	ENSP00000504866.1:n.*747dup
ENST00000680783.1:c.829+7601dup	ENSP00000506329.1:n.829+7601dup
ENST00000681347.1:n.4284dup
ENST00000681514.1:c.*747dup	ENSP00000505963.1:n.*747dup
ENST00000681772.1:c.*1672dup	ENSP00000505829.1:n.*1672dup