Canonical Allele Identifier: CA1139772905

Gene: AGT

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230714126C>A , CM000663.2:g.230714126C>A	GRCh38
NC_000001.10:g.230849872C>A , CM000663.1:g.230849872C>A	GRCh37
NC_000001.9:g.228916495C>A	NCBI36
NG_008836.1:g.5465G>T
NG_008836.2:g.5465G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679684.1:c.-71G>T	ENSP00000505981.1:n.-71G>T
ENST00000679738.1:c.-71G>T	ENSP00000505063.1:n.-71G>T
ENST00000679802.1:c.-71G>T	ENSP00000505184.1:n.-71G>T
ENST00000679854.1:n.441G>T
ENST00000679957.1:c.-71G>T	ENSP00000506646.1:n.-71G>T
ENST00000680041.1:c.-196G>T	ENSP00000504866.1:n.-196G>T
ENST00000680783.1:c.-71G>T	ENSP00000506329.1:n.-71G>T
ENST00000681269.1:c.-30-3273G>T	ENSP00000505985.1:n.-30-3273G>T
ENST00000681347.1:n.441G>T
ENST00000681772.1:c.-71G>T	ENSP00000505829.1:n.-71G>T
ENST00000366667.4:c.-44G>T	ENSP00000355627.4:n.-44G>T
NM_000029.3:c.-44G>T	NP_000020.1:n.-44G>T
NM_001382817.3:c.-30-3273G>T	NP_001369746.2:n.-30-3273G>T