Canonical Allele Identifier: CA2657335
Gene: AGTR1 HGNC NCBI

Linked Data

dbSNP Id: rs780264737

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148741501G>A , CM000665.2:g.148741501G>A GRCh38
NC_000003.11:g.148459288G>A , CM000665.1:g.148459288G>A GRCh37
NC_000003.10:g.149941978G>A NCBI36
NG_008468.1:g.48631G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000349243.8:c.466G>A MANE Select ENSP00000273430.3:p.Ala156Thr
ENST00000402260.2:c.466G>A ENSP00000385641.3:p.Ala156Thr
ENST00000418473.7:c.466G>A ENSP00000398832.4:p.Ala156Thr
ENST00000349243.7:c.466G>A ENSP00000273430.3:p.Ala156Thr
ENST00000402260.1:c.553G>A ENSP00000385641.2:p.Ala185Thr
ENST00000404754.2:c.466G>A ENSP00000385612.2:p.Ala156Thr
ENST00000418473.6:c.571G>A ENSP00000398832.3:p.Ala191Thr
ENST00000461609.1:c.466G>A ENSP00000418851.1:p.Ala156Thr
ENST00000474935.5:c.466G>A ENSP00000418084.1:p.Ala156Thr
ENST00000475347.5:c.466G>A ENSP00000419783.1:p.Ala156Thr
ENST00000497524.5:c.466G>A ENSP00000419422.1:p.Ala156Thr
NM_000685.4:c.466G>A NP_000676.1:p.Ala156Thr
NM_004835.4:c.571G>A NP_004826.5:p.Ala191Thr
NM_009585.3:c.466G>A NP_033611.1:p.Ala156Thr
NM_031850.3:c.571G>A NP_114038.4:p.Ala191Thr
NM_032049.3:c.553G>A NP_114438.2:p.Ala185Thr
NM_000685.5:c.466G>A MANE Select NP_000676.1:p.Ala156Thr
NM_001382736.1:c.466G>A NP_001369665.1:p.Ala156Thr
NM_001382737.1:c.466G>A NP_001369666.1:p.Ala156Thr
NM_004835.5:c.466G>A NP_004826.6:p.Ala156Thr
NM_009585.4:c.466G>A NP_033611.1:p.Ala156Thr
NM_031850.4:c.466G>A NP_114038.5:p.Ala156Thr
NM_032049.4:c.466G>A NP_114438.3:p.Ala156Thr