Canonical Allele Identifier: CA127782
Gene: AGTR1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 18067
ClinVar RCV Id: RCV000019690
dbSNP Id: rs104893677

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148741880C>T , CM000665.2:g.148741880C>T GRCh38
NC_000003.11:g.148459667C>T , CM000665.1:g.148459667C>T GRCh37
NC_000003.10:g.149942357C>T NCBI36
NG_008468.1:g.49010C>T

Transcript Alleles

HGVS Amino-acid change
NM_000685.4:c.845C>T VV NP_000676.1:p.Thr282Met
NM_004835.4:c.950C>T VV NP_004826.5:p.Thr317Met
NM_009585.3:c.845C>T VV NP_033611.1:p.Thr282Met
NM_031850.3:c.950C>T VV NP_114038.4:p.Thr317Met
NM_032049.3:c.932C>T VV NP_114438.2:p.Thr311Met
ENST00000349243.7:c.845C>T ENSP00000273430.3:p.Thr282Met
ENST00000402260.1:c.932C>T ENSP00000385641.2:p.Thr311Met
ENST00000404754.2:c.845C>T ENSP00000385612.2:p.Thr282Met
ENST00000418473.6:n.950C>T ENSP00000398832.3:p.Thr317Met
ENST00000461609.1:c.845C>T ENSP00000418851.1:p.Thr282Met
ENST00000474935.5:c.845C>T ENSP00000418084.1:p.Thr282Met
ENST00000475347.5:c.845C>T ENSP00000419783.1:p.Thr282Met
ENST00000497524.5:c.845C>T ENSP00000419422.1:p.Thr282Met