Canonical Allele Identifier: CA529916133

Gene: AGT

Linked Data

• dbSNP Id: rs1477249955
• gnomAD v2: 1-230839116-T-G
• gnomAD v4: 1-230703370-T-G
• MyVariant Identifiers: chr1:g.230839116T>G (hg19) ; chr1:g.230703370T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230703370T>G , CM000663.2:g.230703370T>G	GRCh38
NC_000001.10:g.230839116T>G , CM000663.1:g.230839116T>G	GRCh37
NC_000001.9:g.228905739T>G	NCBI36
NG_008836.1:g.16221A>C
NG_008836.2:g.16221A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1243-41A>C MANE Select	ENSP00000355627.5:n.1243-41A>C
ENST00000679738.1:c.1243-41A>C	ENSP00000505063.1:n.1243-41A>C
ENST00000679802.1:c.*702-41A>C	ENSP00000505184.1:n.*702-41A>C
ENST00000679854.1:n.5548-41A>C
ENST00000679957.1:c.1234-41A>C	ENSP00000506646.1:n.1234-41A>C
ENST00000680041.1:c.1243-41A>C	ENSP00000504866.1:n.1243-41A>C
ENST00000680783.1:c.829+6625A>C	ENSP00000506329.1:n.829+6625A>C
ENST00000681269.1:c.1243-41A>C	ENSP00000505985.1:n.1243-41A>C
ENST00000681347.1:n.3349-41A>C
ENST00000681514.1:c.1243-41A>C	ENSP00000505963.1:n.1243-41A>C
ENST00000681772.1:c.*737-41A>C	ENSP00000505829.1:n.*737-41A>C
ENST00000366667.4:c.1270-41A>C	ENSP00000355627.4:n.1270-41A>C
NM_000029.3:c.1270-41A>C	NP_000020.1:n.1270-41A>C
NM_000029.4:c.1270-41A>C	NP_000020.1:n.1270-41A>C
NM_001382817.3:c.1243-41A>C	NP_001369746.2:n.1243-41A>C
NM_001384479.1:c.1243-41A>C MANE Select	NP_001371408.1:n.1243-41A>C