Canonical Allele Identifier: CA38867521

Gene: AGT

Linked Data

• dbSNP Id: rs999203794
• MyVariant Identifiers: chr1:g.230841480C>G (hg19) ; chr1:g.230705734C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230705734C>G , CM000663.2:g.230705734C>G	GRCh38
NC_000001.10:g.230841480C>G , CM000663.1:g.230841480C>G	GRCh37
NC_000001.9:g.228908103C>G	NCBI36
NG_008836.1:g.13857G>C
NG_008836.2:g.13857G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1097+199G>C MANE Select	ENSP00000355627.5:n.1097+199G>C
ENST00000679684.1:c.1097+199G>C	ENSP00000505981.1:n.1097+199G>C
ENST00000679738.1:c.1097+199G>C	ENSP00000505063.1:n.1097+199G>C
ENST00000679802.1:c.*556+199G>C	ENSP00000505184.1:n.*556+199G>C
ENST00000679854.1:n.5402+199G>C
ENST00000679957.1:c.1097+199G>C	ENSP00000506646.1:n.1097+199G>C
ENST00000680041.1:c.1097+199G>C	ENSP00000504866.1:n.1097+199G>C
ENST00000680783.1:c.829+4261G>C	ENSP00000506329.1:n.829+4261G>C
ENST00000681269.1:c.1097+199G>C	ENSP00000505985.1:n.1097+199G>C
ENST00000681347.1:n.1807G>C
ENST00000681514.1:c.1097+199G>C	ENSP00000505963.1:n.1097+199G>C
ENST00000681772.1:c.*195G>C	ENSP00000505829.1:n.*195G>C
ENST00000366667.4:c.1124+199G>C	ENSP00000355627.4:n.1124+199G>C
NM_000029.3:c.1124+199G>C	NP_000020.1:n.1124+199G>C
NM_000029.4:c.1124+199G>C	NP_000020.1:n.1124+199G>C
NM_001382817.3:c.1097+199G>C	NP_001369746.2:n.1097+199G>C
NM_001384479.1:c.1097+199G>C MANE Select	NP_001371408.1:n.1097+199G>C