Canonical Allele Identifier: CA85499257

Gene: AGTR1

Linked Data

• ClinVar Variation Id: 901993
• ClinVar RCV Id: RCV001148223
• dbSNP Id: rs537789164
• gnomAD v2: 3-148460131-C-T
• gnomAD v3: 3-148742344-C-T
• gnomAD v4: 3-148742344-C-T
• MyVariant Identifiers: chr3:g.148460131C>T (hg19) ; chr3:g.148742344C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148742344C>T , CM000665.2:g.148742344C>T	GRCh38
NC_000003.11:g.148460131C>T , CM000665.1:g.148460131C>T	GRCh37
NC_000003.10:g.149942821C>T	NCBI36
NG_008468.1:g.49474C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.*229C>T MANE Select	ENSP00000273430.3:n.*229C>T
ENST00000402260.2:c.*229C>T	ENSP00000385641.3:n.*229C>T
ENST00000418473.7:c.*229C>T	ENSP00000398832.4:n.*229C>T
ENST00000349243.7:c.*229C>T	ENSP00000273430.3:n.*229C>T
ENST00000402260.1:c.*229C>T	ENSP00000385641.2:n.*229C>T
ENST00000404754.2:c.*229C>T	ENSP00000385612.2:n.*229C>T
ENST00000418473.6:c.1414C>T	ENSP00000398832.3:n.1414C>T
ENST00000497524.5:c.*229C>T	ENSP00000419422.1:n.*229C>T
NM_000685.4:c.*229C>T	NP_000676.1:n.*229C>T
NM_004835.4:c.*229C>T	NP_004826.5:n.*229C>T
NM_009585.3:c.*229C>T	NP_033611.1:n.*229C>T
NM_031850.3:c.*229C>T	NP_114038.4:n.*229C>T
NM_032049.3:c.*229C>T	NP_114438.2:n.*229C>T
NM_000685.5:c.*229C>T MANE Select	NP_000676.1:n.*229C>T
NM_001382736.1:c.*229C>T	NP_001369665.1:n.*229C>T
NM_001382737.1:c.*229C>T	NP_001369666.1:n.*229C>T
NM_004835.5:c.*229C>T	NP_004826.6:n.*229C>T
NM_009585.4:c.*229C>T	NP_033611.1:n.*229C>T
NM_031850.4:c.*229C>T	NP_114038.5:n.*229C>T
NM_032049.4:c.*229C>T	NP_114438.3:n.*229C>T