Canonical Allele Identifier: CA1013241123

Gene: AGT

Linked Data

• dbSNP Id: rs1663675770
• gnomAD v3: 1-230714151-T-C
• gnomAD v4: 1-230714151-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230714151T>C , CM000663.2:g.230714151T>C	GRCh38
NC_000001.10:g.230849897T>C , CM000663.1:g.230849897T>C	GRCh37
NC_000001.9:g.228916520T>C	NCBI36
NG_008836.1:g.5440A>G
NG_008836.2:g.5440A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679684.1:c.-96A>G	ENSP00000505981.1:n.-96A>G
ENST00000679738.1:c.-96A>G	ENSP00000505063.1:n.-96A>G
ENST00000679802.1:c.-96A>G	ENSP00000505184.1:n.-96A>G
ENST00000679854.1:n.416A>G
ENST00000679957.1:c.-96A>G	ENSP00000506646.1:n.-96A>G
ENST00000680783.1:c.-96A>G	ENSP00000506329.1:n.-96A>G
ENST00000681269.1:c.-30-3298A>G	ENSP00000505985.1:n.-30-3298A>G
ENST00000681347.1:n.416A>G
ENST00000681772.1:c.-96A>G	ENSP00000505829.1:n.-96A>G
ENST00000366667.4:c.-69A>G	ENSP00000355627.4:n.-69A>G
NM_000029.3:c.-69A>G	NP_000020.1:n.-69A>G
NM_001382817.3:c.-30-3298A>G	NP_001369746.2:n.-30-3298A>G