Canonical Allele Identifier: CA11628964
Gene: AGTR1 HGNC NCBI

Linked Data

dbSNP Id: rs1492097

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148719902G>A , CM000665.2:g.148719902G>A GRCh38
NC_000003.11:g.148437689G>A , CM000665.1:g.148437689G>A GRCh37
NC_000003.10:g.149920379G>A NCBI36
NG_008468.1:g.27032G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000349243.8:c.-48+11875G>A MANE Select ENSP00000273430.3:p.=
ENST00000418473.7:c.-105-10278G>A ENSP00000398832.4:p.=
ENST00000349243.7:c.-48+11875G>A ENSP00000273430.3:p.=
ENST00000404754.2:c.-47-21087G>A ENSP00000385612.2:p.=
ENST00000475166.5:n.217-10278G>A
ENST00000497524.5:c.-47-21087G>A ENSP00000419422.1:p.=
NM_000685.4:c.-48+11875G>A NP_000676.1:p.=
NM_004835.4:c.1-10278G>A NP_004826.5:p.=
NM_009585.3:c.-47-21087G>A NP_033611.1:p.=
NM_031850.3:c.1-10278G>A NP_114038.4:p.=
NM_000685.5:c.-48+11875G>A MANE Select NP_000676.1:p.=
NM_001382736.1:c.-47-21087G>A NP_001369665.1:p.=
NM_001382737.1:c.-48+11875G>A NP_001369666.1:p.=
NM_004835.5:c.-105-10278G>A NP_004826.6:p.=
NM_009585.4:c.-47-21087G>A NP_033611.1:p.=
NM_031850.4:c.-105-10278G>A NP_114038.5:p.=
NM_032049.4:c.-262-10278G>A NP_114438.3:p.=