Canonical Allele Identifier: CA1139658297

Gene: AGTR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148698032T>C , CM000665.2:g.148698032T>C	GRCh38
NC_000003.11:g.148415819T>C , CM000665.1:g.148415819T>C	GRCh37
NC_000003.10:g.149898509T>C	NCBI36
NG_008468.1:g.5162T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.-227T>C MANE Select	ENSP00000273430.3:n.-227T>C
ENST00000418473.7:c.-201T>C	ENSP00000398832.4:n.-201T>C
ENST00000349243.7:c.-227T>C	ENSP00000273430.3:n.-227T>C
ENST00000404754.2:c.-165T>C	ENSP00000385612.2:n.-165T>C
ENST00000497524.5:c.-143T>C	ENSP00000419422.1:n.-143T>C
NM_000685.4:c.-227T>C	NP_000676.1:n.-227T>C
NM_004835.4:c.-96T>C	NP_004826.5:n.-96T>C
NM_009585.3:c.-143T>C	NP_033611.1:n.-143T>C
NM_031850.3:c.-180T>C	NP_114038.4:n.-180T>C
NM_000685.5:c.-227T>C MANE Select	NP_000676.1:n.-227T>C
NM_001382736.1:c.-165T>C	NP_001369665.1:n.-165T>C
NM_001382737.1:c.-249T>C	NP_001369666.1:n.-249T>C
NM_004835.5:c.-201T>C	NP_004826.6:n.-201T>C
NM_009585.4:c.-143T>C	NP_033611.1:n.-143T>C
NM_031850.4:c.-285T>C	NP_114038.5:n.-285T>C
NM_032049.4:c.-358T>C	NP_114438.3:n.-358T>C