Canonical Allele Identifier: CA900522899

Gene: AGTR1

Linked Data

• dbSNP Id: rs1321449206
• gnomAD v3: 3-148725395-A-G
• gnomAD v4: 3-148725395-A-G
• MyVariant Identifiers: chr3:g.148443182A>G (hg19) ; chr3:g.148725395A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148725395A>G , CM000665.2:g.148725395A>G	GRCh38
NC_000003.11:g.148443182A>G , CM000665.1:g.148443182A>G	GRCh37
NC_000003.10:g.149925872A>G	NCBI36
NG_008468.1:g.32525A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000349243.8:c.-47-15594A>G MANE Select	ENSP00000273430.3:n.-47-15594A>G
ENST00000418473.7:c.-105-4785A>G	ENSP00000398832.4:n.-105-4785A>G
ENST00000349243.7:c.-47-15594A>G	ENSP00000273430.3:n.-47-15594A>G
ENST00000404754.2:c.-47-15594A>G	ENSP00000385612.2:n.-47-15594A>G
ENST00000475166.5:n.217-4785A>G
ENST00000497524.5:c.-47-15594A>G	ENSP00000419422.1:n.-47-15594A>G
NM_000685.4:c.-47-15594A>G	NP_000676.1:n.-47-15594A>G
NM_004835.4:c.1-4785A>G	NP_004826.5:n.1-4785A>G
NM_009585.3:c.-47-15594A>G	NP_033611.1:n.-47-15594A>G
NM_031850.3:c.1-4785A>G	NP_114038.4:n.1-4785A>G
NM_000685.5:c.-47-15594A>G MANE Select	NP_000676.1:n.-47-15594A>G
NM_001382736.1:c.-47-15594A>G	NP_001369665.1:n.-47-15594A>G
NM_001382737.1:c.-47-15594A>G	NP_001369666.1:n.-47-15594A>G
NM_004835.5:c.-105-4785A>G	NP_004826.6:n.-105-4785A>G
NM_009585.4:c.-47-15594A>G	NP_033611.1:n.-47-15594A>G
NM_031850.4:c.-105-4785A>G	NP_114038.5:n.-105-4785A>G
NM_032049.4:c.-262-4785A>G	NP_114438.3:n.-262-4785A>G