Canonical Allele Identifier: CA354888728

Gene: AGTR1

Linked Data

• ClinVar Variation Id: 2307617
• ClinVar RCV Id: RCV002883990
• dbSNP Id: rs762800866
• MyVariant Identifiers: chr3:g.148459529A>T (hg19) ; chr3:g.148741742A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148741742A>T , CM000665.2:g.148741742A>T	GRCh38
NC_000003.11:g.148459529A>T , CM000665.1:g.148459529A>T	GRCh37
NC_000003.10:g.149942219A>T	NCBI36
NG_008468.1:g.48872A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.707A>T MANE Select	ENSP00000273430.3:p.Asp236Val
ENST00000402260.2:c.707A>T	ENSP00000385641.3:p.Asp236Val
ENST00000418473.7:c.707A>T	ENSP00000398832.4:p.Asp236Val
ENST00000349243.7:c.707A>T	ENSP00000273430.3:p.Asp236Val
ENST00000402260.1:c.794A>T	ENSP00000385641.2:p.Asp265Val
ENST00000404754.2:c.707A>T	ENSP00000385612.2:p.Asp236Val
ENST00000418473.6:c.812A>T	ENSP00000398832.3:p.Asp271Val
ENST00000461609.1:c.707A>T	ENSP00000418851.1:p.Asp236Val
ENST00000474935.5:c.707A>T	ENSP00000418084.1:p.Asp236Val
ENST00000475347.5:c.707A>T	ENSP00000419783.1:p.Asp236Val
ENST00000497524.5:c.707A>T	ENSP00000419422.1:p.Asp236Val
NM_000685.4:c.707A>T	NP_000676.1:p.Asp236Val
NM_004835.4:c.812A>T	NP_004826.5:p.Asp271Val
NM_009585.3:c.707A>T	NP_033611.1:p.Asp236Val
NM_031850.3:c.812A>T	NP_114038.4:p.Asp271Val
NM_032049.3:c.794A>T	NP_114438.2:p.Asp265Val
NM_000685.5:c.707A>T MANE Select	NP_000676.1:p.Asp236Val
NM_001382736.1:c.707A>T	NP_001369665.1:p.Asp236Val
NM_001382737.1:c.707A>T	NP_001369666.1:p.Asp236Val
NM_004835.5:c.707A>T	NP_004826.6:p.Asp236Val
NM_009585.4:c.707A>T	NP_033611.1:p.Asp236Val
NM_031850.4:c.707A>T	NP_114038.5:p.Asp236Val
NM_032049.4:c.707A>T	NP_114438.3:p.Asp236Val