Canonical Allele Identifier: CA436389821
Gene: AGTR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.148459680C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148741893C>A , CM000665.2:g.148741893C>A GRCh38
NC_000003.11:g.148459680C>A , CM000665.1:g.148459680C>A GRCh37
NC_000003.10:g.149942370C>A NCBI36
NG_008468.1:g.49023C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000349243.8:c.858C>A MANE Select ENSP00000273430.3:p.Ile286=
ENST00000402260.2:c.858C>A ENSP00000385641.3:p.Ile286=
ENST00000418473.7:c.858C>A ENSP00000398832.4:p.Ile286=
ENST00000349243.7:c.858C>A ENSP00000273430.3:p.Ile286=
ENST00000402260.1:c.945C>A ENSP00000385641.2:p.Ile315=
ENST00000404754.2:c.858C>A ENSP00000385612.2:p.Ile286=
ENST00000418473.6:c.963C>A ENSP00000398832.3:p.Ile321=
ENST00000461609.1:c.858C>A ENSP00000418851.1:p.Ile286=
ENST00000474935.5:c.858C>A ENSP00000418084.1:p.Ile286=
ENST00000475347.5:c.858C>A ENSP00000419783.1:p.Ile286=
ENST00000497524.5:c.858C>A ENSP00000419422.1:p.Ile286=
NM_000685.4:c.858C>A NP_000676.1:p.Ile286=
NM_004835.4:c.963C>A NP_004826.5:p.Ile321=
NM_009585.3:c.858C>A NP_033611.1:p.Ile286=
NM_031850.3:c.963C>A NP_114038.4:p.Ile321=
NM_032049.3:c.945C>A NP_114438.2:p.Ile315=
NM_000685.5:c.858C>A MANE Select NP_000676.1:p.Ile286=
NM_001382736.1:c.858C>A NP_001369665.1:p.Ile286=
NM_001382737.1:c.858C>A NP_001369666.1:p.Ile286=
NM_004835.5:c.858C>A NP_004826.6:p.Ile286=
NM_009585.4:c.858C>A NP_033611.1:p.Ile286=
NM_031850.4:c.858C>A NP_114038.5:p.Ile286=
NM_032049.4:c.858C>A NP_114438.3:p.Ile286=