Canonical Allele Identifier: CA10617448

Gene: AGTR1

Linked Data

• ClinVar Variation Id: 343679
• ClinVar RCV Id: RCV000330933
• dbSNP Id: rs886058072
• gnomAD v2: 3-148460153-G-A
• gnomAD v3: 3-148742366-G-A
• gnomAD v4: 3-148742366-G-A
• MyVariant Identifiers: chr3:g.148460153G>A (hg19) ; chr3:g.148742366G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148742366G>A , CM000665.2:g.148742366G>A	GRCh38
NC_000003.11:g.148460153G>A , CM000665.1:g.148460153G>A	GRCh37
NC_000003.10:g.149942843G>A	NCBI36
NG_008468.1:g.49496G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000349243.8:c.*251G>A MANE Select	ENSP00000273430.3:n.*251G>A
ENST00000402260.2:c.*251G>A	ENSP00000385641.3:n.*251G>A
ENST00000418473.7:c.*251G>A	ENSP00000398832.4:n.*251G>A
ENST00000349243.7:c.*251G>A	ENSP00000273430.3:n.*251G>A
ENST00000402260.1:c.*251G>A	ENSP00000385641.2:n.*251G>A
ENST00000404754.2:c.*251G>A	ENSP00000385612.2:n.*251G>A
ENST00000418473.6:c.1436G>A	ENSP00000398832.3:n.1436G>A
ENST00000497524.5:c.*251G>A	ENSP00000419422.1:n.*251G>A
NM_000685.4:c.*251G>A	NP_000676.1:n.*251G>A
NM_004835.4:c.*251G>A	NP_004826.5:n.*251G>A
NM_009585.3:c.*251G>A	NP_033611.1:n.*251G>A
NM_031850.3:c.*251G>A	NP_114038.4:n.*251G>A
NM_032049.3:c.*251G>A	NP_114438.2:n.*251G>A
NM_000685.5:c.*251G>A MANE Select	NP_000676.1:n.*251G>A
NM_001382736.1:c.*251G>A	NP_001369665.1:n.*251G>A
NM_001382737.1:c.*251G>A	NP_001369666.1:n.*251G>A
NM_004835.5:c.*251G>A	NP_004826.6:n.*251G>A
NM_009585.4:c.*251G>A	NP_033611.1:n.*251G>A
NM_031850.4:c.*251G>A	NP_114038.5:n.*251G>A
NM_032049.4:c.*251G>A	NP_114438.3:n.*251G>A