Canonical Allele Identifier: CA127780

Gene: AGTR1

Linked Data

• ClinVar Variation Id: 18065
• ClinVar RCV Id: RCV000019688 ; RCV000374969 ; RCV001723581 ; RCV002482889
• dbSNP Id: rs5186
• ExAC: 3:148459988 A / C
• gnomAD v2: 3-148459988-A-C
• gnomAD v3: 3-148742201-A-C
• gnomAD v4: 3-148742201-A-C
• MyVariant Identifiers: chr3:g.148459988A>C (hg19) ; chr3:g.148742201A>C (hg38)
• PubMed: PMID:8021009 ; PMID:9084931 ; PMID:15042429 ; PMID:17668390

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148742201A>C , CM000665.2:g.148742201A>C	GRCh38
NC_000003.11:g.148459988A>C , CM000665.1:g.148459988A>C	GRCh37
NC_000003.10:g.149942678A>C	NCBI36
NG_008468.1:g.49331A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.*86A>C MANE Select	ENSP00000273430.3:n.*86A>C
ENST00000402260.2:c.*86A>C	ENSP00000385641.3:n.*86A>C
ENST00000418473.7:c.*86A>C	ENSP00000398832.4:n.*86A>C
ENST00000349243.7:c.*86A>C	ENSP00000273430.3:n.*86A>C
ENST00000402260.1:c.*86A>C	ENSP00000385641.2:n.*86A>C
ENST00000404754.2:c.*86A>C	ENSP00000385612.2:n.*86A>C
ENST00000418473.6:c.1271A>C	ENSP00000398832.3:n.1271A>C
ENST00000461609.1:c.*86A>C	ENSP00000418851.1:n.*86A>C
ENST00000474935.5:c.*86A>C	ENSP00000418084.1:n.*86A>C
ENST00000475347.5:c.*86A>C	ENSP00000419783.1:n.*86A>C
ENST00000497524.5:c.*86A>C	ENSP00000419422.1:n.*86A>C
NM_000685.4:c.*86A>C	NP_000676.1:n.*86A>C
NM_004835.4:c.*86A>C	NP_004826.5:n.*86A>C
NM_009585.3:c.*86A>C	NP_033611.1:n.*86A>C
NM_031850.3:c.*86A>C	NP_114038.4:n.*86A>C
NM_032049.3:c.*86A>C	NP_114438.2:n.*86A>C
NM_000685.5:c.*86A>C MANE Select	NP_000676.1:n.*86A>C
NM_001382736.1:c.*86A>C	NP_001369665.1:n.*86A>C
NM_001382737.1:c.*86A>C	NP_001369666.1:n.*86A>C
NM_004835.5:c.*86A>C	NP_004826.6:n.*86A>C
NM_009585.4:c.*86A>C	NP_033611.1:n.*86A>C
NM_031850.4:c.*86A>C	NP_114038.5:n.*86A>C
NM_032049.4:c.*86A>C	NP_114438.3:n.*86A>C