Canonical Allele Identifier: CA10615050

Gene: AGTR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148697928C>G , CM000665.2:g.148697928C>G	GRCh38
NC_000003.11:g.148415715C>G , CM000665.1:g.148415715C>G	GRCh37
NC_000003.10:g.149898405C>G	NCBI36
NG_008468.1:g.5058C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.-331C>G MANE Select	ENSP00000273430.3:n.-331C>G
ENST00000418473.7:c.-305C>G	ENSP00000398832.4:n.-305C>G
ENST00000349243.7:c.-331C>G	ENSP00000273430.3:n.-331C>G
ENST00000404754.2:c.-269C>G	ENSP00000385612.2:n.-269C>G
ENST00000497524.5:c.-247C>G	ENSP00000419422.1:n.-247C>G
NM_000685.4:c.-331C>G	NP_000676.1:n.-331C>G
NM_004835.4:c.-200C>G	NP_004826.5:n.-200C>G
NM_009585.3:c.-247C>G	NP_033611.1:n.-247C>G
NM_031850.3:c.-284C>G	NP_114038.4:n.-284C>G
NM_000685.5:c.-331C>G MANE Select	NP_000676.1:n.-331C>G
NM_001382736.1:c.-269C>G	NP_001369665.1:n.-269C>G
NM_001382737.1:c.-353C>G	NP_001369666.1:n.-353C>G
NM_004835.5:c.-305C>G	NP_004826.6:n.-305C>G
NM_009585.4:c.-247C>G	NP_033611.1:n.-247C>G
NM_031850.4:c.-389C>G	NP_114038.5:n.-389C>G
NM_032049.4:c.-462C>G	NP_114438.3:n.-462C>G