Canonical Allele Identifier: CA436389829

Gene: AGTR1

Linked Data

• MyVariant Identifiers: chr3:g.148459683C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148741896C>A , CM000665.2:g.148741896C>A	GRCh38
NC_000003.11:g.148459683C>A , CM000665.1:g.148459683C>A	GRCh37
NC_000003.10:g.149942373C>A	NCBI36
NG_008468.1:g.49026C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.861C>A MANE Select	ENSP00000273430.3:p.Thr287=
ENST00000402260.2:c.861C>A	ENSP00000385641.3:p.Thr287=
ENST00000418473.7:c.861C>A	ENSP00000398832.4:p.Thr287=
ENST00000349243.7:c.861C>A	ENSP00000273430.3:p.Thr287=
ENST00000402260.1:c.948C>A	ENSP00000385641.2:p.Thr316=
ENST00000404754.2:c.861C>A	ENSP00000385612.2:p.Thr287=
ENST00000418473.6:c.966C>A	ENSP00000398832.3:p.Thr322=
ENST00000461609.1:c.861C>A	ENSP00000418851.1:p.Thr287=
ENST00000474935.5:c.861C>A	ENSP00000418084.1:p.Thr287=
ENST00000475347.5:c.861C>A	ENSP00000419783.1:p.Thr287=
ENST00000497524.5:c.861C>A	ENSP00000419422.1:p.Thr287=
NM_000685.4:c.861C>A	NP_000676.1:p.Thr287=
NM_004835.4:c.966C>A	NP_004826.5:p.Thr322=
NM_009585.3:c.861C>A	NP_033611.1:p.Thr287=
NM_031850.3:c.966C>A	NP_114038.4:p.Thr322=
NM_032049.3:c.948C>A	NP_114438.2:p.Thr316=
NM_000685.5:c.861C>A MANE Select	NP_000676.1:p.Thr287=
NM_001382736.1:c.861C>A	NP_001369665.1:p.Thr287=
NM_001382737.1:c.861C>A	NP_001369666.1:p.Thr287=
NM_004835.5:c.861C>A	NP_004826.6:p.Thr287=
NM_009585.4:c.861C>A	NP_033611.1:p.Thr287=
NM_031850.4:c.861C>A	NP_114038.5:p.Thr287=
NM_032049.4:c.861C>A	NP_114438.3:p.Thr287=