Canonical Allele Identifier: CA354889226

Gene: AGTR1

Linked Data

• ClinVar Variation Id: 900271
• ClinVar RCV Id: RCV001145359
• dbSNP Id: rs1218342417
• MyVariant Identifiers: chr3:g.148459637G>C (hg19) ; chr3:g.148741850G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148741850G>C , CM000665.2:g.148741850G>C	GRCh38
NC_000003.11:g.148459637G>C , CM000665.1:g.148459637G>C	GRCh37
NC_000003.10:g.149942327G>C	NCBI36
NG_008468.1:g.48980G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.815G>C MANE Select	ENSP00000273430.3:p.Arg272Pro
ENST00000402260.2:c.815G>C	ENSP00000385641.3:p.Arg272Pro
ENST00000418473.7:c.815G>C	ENSP00000398832.4:p.Arg272Pro
ENST00000349243.7:c.815G>C	ENSP00000273430.3:p.Arg272Pro
ENST00000402260.1:c.902G>C	ENSP00000385641.2:p.Arg301Pro
ENST00000404754.2:c.815G>C	ENSP00000385612.2:p.Arg272Pro
ENST00000418473.6:c.920G>C	ENSP00000398832.3:p.Arg307Pro
ENST00000461609.1:c.815G>C	ENSP00000418851.1:p.Arg272Pro
ENST00000474935.5:c.815G>C	ENSP00000418084.1:p.Arg272Pro
ENST00000475347.5:c.815G>C	ENSP00000419783.1:p.Arg272Pro
ENST00000497524.5:c.815G>C	ENSP00000419422.1:p.Arg272Pro
NM_000685.4:c.815G>C	NP_000676.1:p.Arg272Pro
NM_004835.4:c.920G>C	NP_004826.5:p.Arg307Pro
NM_009585.3:c.815G>C	NP_033611.1:p.Arg272Pro
NM_031850.3:c.920G>C	NP_114038.4:p.Arg307Pro
NM_032049.3:c.902G>C	NP_114438.2:p.Arg301Pro
NM_000685.5:c.815G>C MANE Select	NP_000676.1:p.Arg272Pro
NM_001382736.1:c.815G>C	NP_001369665.1:p.Arg272Pro
NM_001382737.1:c.815G>C	NP_001369666.1:p.Arg272Pro
NM_004835.5:c.815G>C	NP_004826.6:p.Arg272Pro
NM_009585.4:c.815G>C	NP_033611.1:p.Arg272Pro
NM_031850.4:c.815G>C	NP_114038.5:p.Arg272Pro
NM_032049.4:c.815G>C	NP_114438.3:p.Arg272Pro