Canonical Allele Identifier: CA2657439
Gene: AGTR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1920250
ClinVar RCV Id: RCV002591054
dbSNP Id: rs755384581

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148742089C>T , CM000665.2:g.148742089C>T GRCh38
NC_000003.11:g.148459876C>T , CM000665.1:g.148459876C>T GRCh37
NC_000003.10:g.149942566C>T NCBI36
NG_008468.1:g.49219C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000349243.8:c.1054C>T MANE Select ENSP00000273430.3:p.Pro352Ser
ENST00000402260.2:c.1054C>T ENSP00000385641.3:p.Pro352Ser
ENST00000418473.7:c.1054C>T ENSP00000398832.4:p.Pro352Ser
ENST00000349243.7:c.1054C>T ENSP00000273430.3:p.Pro352Ser
ENST00000402260.1:c.1141C>T ENSP00000385641.2:p.Pro381Ser
ENST00000404754.2:c.1054C>T ENSP00000385612.2:p.Pro352Ser
ENST00000418473.6:c.1159C>T ENSP00000398832.3:p.Pro387Ser
ENST00000461609.1:c.1054C>T ENSP00000418851.1:p.Pro352Ser
ENST00000474935.5:c.1054C>T ENSP00000418084.1:p.Pro352Ser
ENST00000475347.5:c.1054C>T ENSP00000419783.1:p.Pro352Ser
ENST00000497524.5:c.1054C>T ENSP00000419422.1:p.Pro352Ser
NM_000685.4:c.1054C>T NP_000676.1:p.Pro352Ser
NM_004835.4:c.1159C>T NP_004826.5:p.Pro387Ser
NM_009585.3:c.1054C>T NP_033611.1:p.Pro352Ser
NM_031850.3:c.1159C>T NP_114038.4:p.Pro387Ser
NM_032049.3:c.1141C>T NP_114438.2:p.Pro381Ser
NM_000685.5:c.1054C>T MANE Select NP_000676.1:p.Pro352Ser
NM_001382736.1:c.1054C>T NP_001369665.1:p.Pro352Ser
NM_001382737.1:c.1054C>T NP_001369666.1:p.Pro352Ser
NM_004835.5:c.1054C>T NP_004826.6:p.Pro352Ser
NM_009585.4:c.1054C>T NP_033611.1:p.Pro352Ser
NM_031850.4:c.1054C>T NP_114038.5:p.Pro352Ser
NM_032049.4:c.1054C>T NP_114438.3:p.Pro352Ser