Canonical Allele Identifier: CA900522209

Gene: AGTR1

Linked Data

• dbSNP Id: rs1492097
• gnomAD v3: 3-148719902-G-T
• gnomAD v4: 3-148719902-G-T
• MyVariant Identifiers: chr3:g.148437689G>T (hg19) ; chr3:g.148719902G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148719902G>T , CM000665.2:g.148719902G>T	GRCh38
NC_000003.11:g.148437689G>T , CM000665.1:g.148437689G>T	GRCh37
NC_000003.10:g.149920379G>T	NCBI36
NG_008468.1:g.27032G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000349243.8:c.-48+11875G>T MANE Select	ENSP00000273430.3:n.-48+11875G>T
ENST00000418473.7:c.-105-10278G>T	ENSP00000398832.4:n.-105-10278G>T
ENST00000349243.7:c.-48+11875G>T	ENSP00000273430.3:n.-48+11875G>T
ENST00000404754.2:c.-47-21087G>T	ENSP00000385612.2:n.-47-21087G>T
ENST00000475166.5:n.217-10278G>T
ENST00000497524.5:c.-47-21087G>T	ENSP00000419422.1:n.-47-21087G>T
NM_000685.4:c.-48+11875G>T	NP_000676.1:n.-48+11875G>T
NM_004835.4:c.1-10278G>T	NP_004826.5:n.1-10278G>T
NM_009585.3:c.-47-21087G>T	NP_033611.1:n.-47-21087G>T
NM_031850.3:c.1-10278G>T	NP_114038.4:n.1-10278G>T
NM_000685.5:c.-48+11875G>T MANE Select	NP_000676.1:n.-48+11875G>T
NM_001382736.1:c.-47-21087G>T	NP_001369665.1:n.-47-21087G>T
NM_001382737.1:c.-48+11875G>T	NP_001369666.1:n.-48+11875G>T
NM_004835.5:c.-105-10278G>T	NP_004826.6:n.-105-10278G>T
NM_009585.4:c.-47-21087G>T	NP_033611.1:n.-47-21087G>T
NM_031850.4:c.-105-10278G>T	NP_114038.5:n.-105-10278G>T
NM_032049.4:c.-262-10278G>T	NP_114438.3:n.-262-10278G>T