Canonical Allele Identifier: CA1409900563
Gene: AGTR1 HGNC NCBI

Linked Data

dbSNP Id: rs1713048494

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148712498A>C , CM000665.2:g.148712498A>C GRCh38
NC_000003.11:g.148430285A>C , CM000665.1:g.148430285A>C GRCh37
NC_000003.10:g.149912975A>C NCBI36
NG_008468.1:g.19628A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000349243.8:c.-48+4471A>C MANE Select ENSP00000273430.3:n.-48+4471A>C
ENST00000418473.7:c.-106+14371A>C ENSP00000398832.4:n.-106+14371A>C
ENST00000349243.7:c.-48+4471A>C ENSP00000273430.3:n.-48+4471A>C
ENST00000404754.2:c.-48+14349A>C ENSP00000385612.2:n.-48+14349A>C
ENST00000475166.5:n.216+4471A>C
ENST00000497524.5:c.-48+14371A>C ENSP00000419422.1:n.-48+14371A>C
NM_000685.4:c.-48+4471A>C NP_000676.1:n.-48+4471A>C
NM_004835.4:c.-1+14371A>C NP_004826.5:n.-1+14371A>C
NM_009585.3:c.-48+14371A>C NP_033611.1:n.-48+14371A>C
NM_031850.3:c.-1+4471A>C NP_114038.4:n.-1+4471A>C
NM_000685.5:c.-48+4471A>C MANE Select NP_000676.1:n.-48+4471A>C
NM_001382736.1:c.-48+14349A>C NP_001369665.1:n.-48+14349A>C
NM_001382737.1:c.-48+4471A>C NP_001369666.1:n.-48+4471A>C
NM_004835.5:c.-106+14371A>C NP_004826.6:n.-106+14371A>C
NM_009585.4:c.-48+14371A>C NP_033611.1:n.-48+14371A>C
NM_031850.4:c.-106+4471A>C NP_114038.5:n.-106+4471A>C
NM_032049.4:c.-263+14371A>C NP_114438.3:n.-263+14371A>C