Canonical Allele Identifier: CA38867532

Gene: AGT

Linked Data

• dbSNP Id: rs546168030
• gnomAD v3: 1-230705758-T-C
• gnomAD v4: 1-230705758-T-C
• MyVariant Identifiers: chr1:g.230841504T>C (hg19) ; chr1:g.230705758T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230705758T>C , CM000663.2:g.230705758T>C	GRCh38
NC_000001.10:g.230841504T>C , CM000663.1:g.230841504T>C	GRCh37
NC_000001.9:g.228908127T>C	NCBI36
NG_008836.1:g.13833A>G
NG_008836.2:g.13833A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1097+175A>G MANE Select	ENSP00000355627.5:n.1097+175A>G
ENST00000679684.1:c.1097+175A>G	ENSP00000505981.1:n.1097+175A>G
ENST00000679738.1:c.1097+175A>G	ENSP00000505063.1:n.1097+175A>G
ENST00000679802.1:c.*556+175A>G	ENSP00000505184.1:n.*556+175A>G
ENST00000679854.1:n.5402+175A>G
ENST00000679957.1:c.1097+175A>G	ENSP00000506646.1:n.1097+175A>G
ENST00000680041.1:c.1097+175A>G	ENSP00000504866.1:n.1097+175A>G
ENST00000680783.1:c.829+4237A>G	ENSP00000506329.1:n.829+4237A>G
ENST00000681269.1:c.1097+175A>G	ENSP00000505985.1:n.1097+175A>G
ENST00000681347.1:n.1783A>G
ENST00000681514.1:c.1097+175A>G	ENSP00000505963.1:n.1097+175A>G
ENST00000681772.1:c.*171A>G	ENSP00000505829.1:n.*171A>G
ENST00000366667.4:c.1124+175A>G	ENSP00000355627.4:n.1124+175A>G
NM_000029.3:c.1124+175A>G	NP_000020.1:n.1124+175A>G
NM_000029.4:c.1124+175A>G	NP_000020.1:n.1124+175A>G
NM_001382817.3:c.1097+175A>G	NP_001369746.2:n.1097+175A>G
NM_001384479.1:c.1097+175A>G MANE Select	NP_001371408.1:n.1097+175A>G