Canonical Allele Identifier: CA1409904258
Gene: AGTR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148719967G= , CM000665.2:g.148719967G= GRCh38
NC_000003.11:g.148437754G= , CM000665.1:g.148437754G= GRCh37
NC_000003.10:g.149920444G= NCBI36
NG_008468.1:g.27097G=

Transcript Alleles

HGVS Amino-acid change
ENST00000349243.8:c.-48+11940G= MANE Select ENSP00000273430.3:n.-48+11940G=
ENST00000418473.7:c.-105-10213G= ENSP00000398832.4:n.-105-10213G=
ENST00000349243.7:c.-48+11940G= ENSP00000273430.3:n.-48+11940G=
ENST00000404754.2:c.-47-21022G= ENSP00000385612.2:n.-47-21022G=
ENST00000475166.5:n.217-10213G=
ENST00000497524.5:c.-47-21022G= ENSP00000419422.1:n.-47-21022G=
NM_000685.4:c.-48+11940G= NP_000676.1:n.-48+11940G=
NM_004835.4:c.1-10213G= NP_004826.5:n.1-10213G=
NM_009585.3:c.-47-21022G= NP_033611.1:n.-47-21022G=
NM_031850.3:c.1-10213G= NP_114038.4:n.1-10213G=
NM_000685.5:c.-48+11940G= MANE Select NP_000676.1:n.-48+11940G=
NM_001382736.1:c.-47-21022G= NP_001369665.1:n.-47-21022G=
NM_001382737.1:c.-48+11940G= NP_001369666.1:n.-48+11940G=
NM_004835.5:c.-105-10213G= NP_004826.6:n.-105-10213G=
NM_009585.4:c.-47-21022G= NP_033611.1:n.-47-21022G=
NM_031850.4:c.-105-10213G= NP_114038.5:n.-105-10213G=
NM_032049.4:c.-262-10213G= NP_114438.3:n.-262-10213G=