Canonical Allele Identifier: CA2607358065

Gene: AGT

Linked Data

• dbSNP Id: rs1434378577
• gnomAD v3: 1-230714144-C-T
• gnomAD v4: 1-230714144-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230714144C>T , CM000663.2:g.230714144C>T	GRCh38
NC_000001.10:g.230849890C>T , CM000663.1:g.230849890C>T	GRCh37
NC_000001.9:g.228916513C>T	NCBI36
NG_008836.1:g.5447G>A
NG_008836.2:g.5447G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679684.1:c.-89G>A	ENSP00000505981.1:n.-89G>A
ENST00000679738.1:c.-89G>A	ENSP00000505063.1:n.-89G>A
ENST00000679802.1:c.-89G>A	ENSP00000505184.1:n.-89G>A
ENST00000679854.1:n.423G>A
ENST00000679957.1:c.-89G>A	ENSP00000506646.1:n.-89G>A
ENST00000680041.1:c.-214G>A	ENSP00000504866.1:n.-214G>A
ENST00000680783.1:c.-89G>A	ENSP00000506329.1:n.-89G>A
ENST00000681269.1:c.-30-3291G>A	ENSP00000505985.1:n.-30-3291G>A
ENST00000681347.1:n.423G>A
ENST00000681772.1:c.-89G>A	ENSP00000505829.1:n.-89G>A
ENST00000366667.4:c.-62G>A	ENSP00000355627.4:n.-62G>A
NM_000029.3:c.-62G>A	NP_000020.1:n.-62G>A
NM_001382817.3:c.-30-3291G>A	NP_001369746.2:n.-30-3291G>A