Canonical Allele Identifier: CA85497688

Gene: AGTR1

Linked Data

• dbSNP Id: rs995803867
• gnomAD v2: 3-148459231-C-T
• gnomAD v3: 3-148741444-C-T
• gnomAD v4: 3-148741444-C-T
• COSMIC: COSM1182247
• MyVariant Identifiers: chr3:g.148459231C>T (hg19) ; chr3:g.148741444C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148741444C>T , CM000665.2:g.148741444C>T	GRCh38
NC_000003.11:g.148459231C>T , CM000665.1:g.148459231C>T	GRCh37
NC_000003.10:g.149941921C>T	NCBI36
NG_008468.1:g.48574C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.409C>T MANE Select	ENSP00000273430.3:p.Arg137Cys
ENST00000402260.2:c.409C>T	ENSP00000385641.3:p.Arg137Cys
ENST00000418473.7:c.409C>T	ENSP00000398832.4:p.Arg137Cys
ENST00000349243.7:c.409C>T	ENSP00000273430.3:p.Arg137Cys
ENST00000402260.1:c.496C>T	ENSP00000385641.2:p.Arg166Cys
ENST00000404754.2:c.409C>T	ENSP00000385612.2:p.Arg137Cys
ENST00000418473.6:c.514C>T	ENSP00000398832.3:p.Arg172Cys
ENST00000461609.1:c.409C>T	ENSP00000418851.1:p.Arg137Cys
ENST00000474935.5:c.409C>T	ENSP00000418084.1:p.Arg137Cys
ENST00000475347.5:c.409C>T	ENSP00000419783.1:p.Arg137Cys
ENST00000497524.5:c.409C>T	ENSP00000419422.1:p.Arg137Cys
NM_000685.4:c.409C>T	NP_000676.1:p.Arg137Cys
NM_004835.4:c.514C>T	NP_004826.5:p.Arg172Cys
NM_009585.3:c.409C>T	NP_033611.1:p.Arg137Cys
NM_031850.3:c.514C>T	NP_114038.4:p.Arg172Cys
NM_032049.3:c.496C>T	NP_114438.2:p.Arg166Cys
NM_000685.5:c.409C>T MANE Select	NP_000676.1:p.Arg137Cys
NM_001382736.1:c.409C>T	NP_001369665.1:p.Arg137Cys
NM_001382737.1:c.409C>T	NP_001369666.1:p.Arg137Cys
NM_004835.5:c.409C>T	NP_004826.6:p.Arg137Cys
NM_009585.4:c.409C>T	NP_033611.1:p.Arg137Cys
NM_031850.4:c.409C>T	NP_114038.5:p.Arg137Cys
NM_032049.4:c.409C>T	NP_114438.3:p.Arg137Cys