Canonical Allele Identifier: CA85562097

Gene: AGTR1

Linked Data

• dbSNP Id: rs916928574
• gnomAD v3: 3-148708605-T-C
• gnomAD v4: 3-148708605-T-C
• MyVariant Identifiers: chr3:g.148426392T>C (hg19) ; chr3:g.148708605T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148708605T>C , CM000665.2:g.148708605T>C	GRCh38
NC_000003.11:g.148426392T>C , CM000665.1:g.148426392T>C	GRCh37
NC_000003.10:g.149909082T>C	NCBI36
NG_008468.1:g.15735T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.-48+578T>C MANE Select	ENSP00000273430.3:n.-48+578T>C
ENST00000418473.7:c.-106+10478T>C	ENSP00000398832.4:n.-106+10478T>C
ENST00000349243.7:c.-48+578T>C	ENSP00000273430.3:n.-48+578T>C
ENST00000404754.2:c.-48+10456T>C	ENSP00000385612.2:n.-48+10456T>C
ENST00000475166.5:n.216+578T>C
ENST00000497524.5:c.-48+10478T>C	ENSP00000419422.1:n.-48+10478T>C
NM_000685.4:c.-48+578T>C	NP_000676.1:n.-48+578T>C
NM_004835.4:c.-1+10478T>C	NP_004826.5:n.-1+10478T>C
NM_009585.3:c.-48+10478T>C	NP_033611.1:n.-48+10478T>C
NM_031850.3:c.-1+578T>C	NP_114038.4:n.-1+578T>C
NM_000685.5:c.-48+578T>C MANE Select	NP_000676.1:n.-48+578T>C
NM_001382736.1:c.-48+10456T>C	NP_001369665.1:n.-48+10456T>C
NM_001382737.1:c.-48+578T>C	NP_001369666.1:n.-48+578T>C
NM_004835.5:c.-106+10478T>C	NP_004826.6:n.-106+10478T>C
NM_009585.4:c.-48+10478T>C	NP_033611.1:n.-48+10478T>C
NM_031850.4:c.-106+578T>C	NP_114038.5:n.-106+578T>C
NM_032049.4:c.-263+10478T>C	NP_114438.3:n.-263+10478T>C