Canonical Allele Identifier: CA85499269

Gene: AGTR1

Linked Data

• dbSNP Id: rs547202236
• gnomAD v2: 3-148460155-T-C
• gnomAD v3: 3-148742368-T-C
• gnomAD v4: 3-148742368-T-C
• MyVariant Identifiers: chr3:g.148460155T>C (hg19) ; chr3:g.148742368T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148742368T>C , CM000665.2:g.148742368T>C	GRCh38
NC_000003.11:g.148460155T>C , CM000665.1:g.148460155T>C	GRCh37
NC_000003.10:g.149942845T>C	NCBI36
NG_008468.1:g.49498T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.*253T>C MANE Select	ENSP00000273430.3:n.*253T>C
ENST00000402260.2:c.*253T>C	ENSP00000385641.3:n.*253T>C
ENST00000418473.7:c.*253T>C	ENSP00000398832.4:n.*253T>C
ENST00000349243.7:c.*253T>C	ENSP00000273430.3:n.*253T>C
ENST00000402260.1:c.*253T>C	ENSP00000385641.2:n.*253T>C
ENST00000404754.2:c.*253T>C	ENSP00000385612.2:n.*253T>C
ENST00000418473.6:c.1438T>C	ENSP00000398832.3:n.1438T>C
ENST00000497524.5:c.*253T>C	ENSP00000419422.1:n.*253T>C
NM_000685.4:c.*253T>C	NP_000676.1:n.*253T>C
NM_004835.4:c.*253T>C	NP_004826.5:n.*253T>C
NM_009585.3:c.*253T>C	NP_033611.1:n.*253T>C
NM_031850.3:c.*253T>C	NP_114038.4:n.*253T>C
NM_032049.3:c.*253T>C	NP_114438.2:n.*253T>C
NM_000685.5:c.*253T>C MANE Select	NP_000676.1:n.*253T>C
NM_001382736.1:c.*253T>C	NP_001369665.1:n.*253T>C
NM_001382737.1:c.*253T>C	NP_001369666.1:n.*253T>C
NM_004835.5:c.*253T>C	NP_004826.6:n.*253T>C
NM_009585.4:c.*253T>C	NP_033611.1:n.*253T>C
NM_031850.4:c.*253T>C	NP_114038.5:n.*253T>C
NM_032049.4:c.*253T>C	NP_114438.3:n.*253T>C