Canonical Allele Identifier: CA546915308

Gene: AGTR1

Linked Data

• dbSNP Id: rs1281131705
• gnomAD v2: 3-148460075-CT-C
• gnomAD v3: 3-148742288-CT-C
• gnomAD v4: 3-148742288-CT-C
• MyVariant Identifiers: chr3:g.148460076del (hg19) ; chr3:g.148742289del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148742292del , CM000665.2:g.148742292del	GRCh38
NC_000003.11:g.148460079del , CM000665.1:g.148460079del	GRCh37
NC_000003.10:g.149942769del	NCBI36
NG_008468.1:g.49422del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.*177del MANE Select	ENSP00000273430.3:n.*177del
ENST00000402260.2:c.*177del	ENSP00000385641.3:n.*177del
ENST00000418473.7:c.*177del	ENSP00000398832.4:n.*177del
ENST00000349243.7:c.*177del	ENSP00000273430.3:n.*177del
ENST00000402260.1:c.*177del	ENSP00000385641.2:n.*177del
ENST00000404754.2:c.*177del	ENSP00000385612.2:n.*177del
ENST00000418473.6:c.1362del	ENSP00000398832.3:n.1362del
ENST00000497524.5:c.*177del	ENSP00000419422.1:n.*177del
NM_000685.4:c.*177del	NP_000676.1:n.*177del
NM_004835.4:c.*177del	NP_004826.5:n.*177del
NM_009585.3:c.*177del	NP_033611.1:n.*177del
NM_031850.3:c.*177del	NP_114038.4:n.*177del
NM_032049.3:c.*177del	NP_114438.2:n.*177del
NM_000685.5:c.*177del MANE Select	NP_000676.1:n.*177del
NM_001382736.1:c.*177del	NP_001369665.1:n.*177del
NM_001382737.1:c.*177del	NP_001369666.1:n.*177del
NM_004835.5:c.*177del	NP_004826.6:n.*177del
NM_009585.4:c.*177del	NP_033611.1:n.*177del
NM_031850.4:c.*177del	NP_114038.5:n.*177del
NM_032049.4:c.*177del	NP_114438.3:n.*177del