Canonical Allele Identifier: CA11513386
Gene: AGTR1 HGNC NCBI

Linked Data

dbSNP Id: rs12695895

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148725481C>T , CM000665.2:g.148725481C>T GRCh38
NC_000003.11:g.148443268C>T , CM000665.1:g.148443268C>T GRCh37
NC_000003.10:g.149925958C>T NCBI36
NG_008468.1:g.32611C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000349243.8:c.-47-15508C>T MANE Select ENSP00000273430.3:n.-47-15508C>T
ENST00000418473.7:c.-105-4699C>T ENSP00000398832.4:n.-105-4699C>T
ENST00000349243.7:c.-47-15508C>T ENSP00000273430.3:n.-47-15508C>T
ENST00000404754.2:c.-47-15508C>T ENSP00000385612.2:n.-47-15508C>T
ENST00000475166.5:n.217-4699C>T
ENST00000497524.5:c.-47-15508C>T ENSP00000419422.1:n.-47-15508C>T
NM_000685.4:c.-47-15508C>T NP_000676.1:n.-47-15508C>T
NM_004835.4:c.1-4699C>T NP_004826.5:n.1-4699C>T
NM_009585.3:c.-47-15508C>T NP_033611.1:n.-47-15508C>T
NM_031850.3:c.1-4699C>T NP_114038.4:n.1-4699C>T
NM_000685.5:c.-47-15508C>T MANE Select NP_000676.1:n.-47-15508C>T
NM_001382736.1:c.-47-15508C>T NP_001369665.1:n.-47-15508C>T
NM_001382737.1:c.-47-15508C>T NP_001369666.1:n.-47-15508C>T
NM_004835.5:c.-105-4699C>T NP_004826.6:n.-105-4699C>T
NM_009585.4:c.-47-15508C>T NP_033611.1:n.-47-15508C>T
NM_031850.4:c.-105-4699C>T NP_114038.5:n.-105-4699C>T
NM_032049.4:c.-262-4699C>T NP_114438.3:n.-262-4699C>T