Canonical Allele Identifier: CA38874754

Gene: AGT

Linked Data

• dbSNP Id: rs984491800
• gnomAD v2: 1-230849134-A-G
• gnomAD v3: 1-230713388-A-G
• gnomAD v4: 1-230713388-A-G
• MyVariant Identifiers: chr1:g.230849134A>G (hg19) ; chr1:g.230713388A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230713388A>G , CM000663.2:g.230713388A>G	GRCh38
NC_000001.10:g.230849134A>G , CM000663.1:g.230849134A>G	GRCh37
NC_000001.9:g.228915757A>G	NCBI36
NG_008836.1:g.6203T>C
NG_008836.2:g.6203T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.-31+698T>C MANE Select	ENSP00000355627.5:n.-31+698T>C
ENST00000679684.1:c.-31+698T>C	ENSP00000505981.1:n.-31+698T>C
ENST00000679738.1:c.-31+698T>C	ENSP00000505063.1:n.-31+698T>C
ENST00000679802.1:c.-31+698T>C	ENSP00000505184.1:n.-31+698T>C
ENST00000679854.1:n.481+698T>C
ENST00000679957.1:c.-31+698T>C	ENSP00000506646.1:n.-31+698T>C
ENST00000680041.1:c.-156+698T>C	ENSP00000504866.1:n.-156+698T>C
ENST00000680783.1:c.-31+698T>C	ENSP00000506329.1:n.-31+698T>C
ENST00000681269.1:c.-30-2535T>C	ENSP00000505985.1:n.-30-2535T>C
ENST00000681347.1:n.481+698T>C
ENST00000681514.1:c.-117-19T>C	ENSP00000505963.1:n.-117-19T>C
ENST00000681772.1:c.-31+698T>C	ENSP00000505829.1:n.-31+698T>C
ENST00000366667.4:c.-4+698T>C	ENSP00000355627.4:n.-4+698T>C
NM_000029.3:c.-4+698T>C	NP_000020.1:n.-4+698T>C
NM_000029.4:c.-4+698T>C	NP_000020.1:n.-4+698T>C
NM_001382817.3:c.-30-2535T>C	NP_001369746.2:n.-30-2535T>C
NM_001384479.1:c.-31+698T>C MANE Select	NP_001371408.1:n.-31+698T>C