Canonical Allele Identifier: CA1054776307
Gene: AGTR1 HGNC NCBI

Linked Data

dbSNP Id: rs1713872766

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148725435T>A , CM000665.2:g.148725435T>A GRCh38
NC_000003.11:g.148443222T>A , CM000665.1:g.148443222T>A GRCh37
NC_000003.10:g.149925912T>A NCBI36
NG_008468.1:g.32565T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000349243.8:c.-47-15554T>A MANE Select ENSP00000273430.3:n.-47-15554T>A
ENST00000418473.7:c.-105-4745T>A ENSP00000398832.4:n.-105-4745T>A
ENST00000349243.7:c.-47-15554T>A ENSP00000273430.3:n.-47-15554T>A
ENST00000404754.2:c.-47-15554T>A ENSP00000385612.2:n.-47-15554T>A
ENST00000475166.5:n.217-4745T>A
ENST00000497524.5:c.-47-15554T>A ENSP00000419422.1:n.-47-15554T>A
NM_000685.4:c.-47-15554T>A NP_000676.1:n.-47-15554T>A
NM_004835.4:c.1-4745T>A NP_004826.5:n.1-4745T>A
NM_009585.3:c.-47-15554T>A NP_033611.1:n.-47-15554T>A
NM_031850.3:c.1-4745T>A NP_114038.4:n.1-4745T>A
NM_000685.5:c.-47-15554T>A MANE Select NP_000676.1:n.-47-15554T>A
NM_001382736.1:c.-47-15554T>A NP_001369665.1:n.-47-15554T>A
NM_001382737.1:c.-47-15554T>A NP_001369666.1:n.-47-15554T>A
NM_004835.5:c.-105-4745T>A NP_004826.6:n.-105-4745T>A
NM_009585.4:c.-47-15554T>A NP_033611.1:n.-47-15554T>A
NM_031850.4:c.-105-4745T>A NP_114038.5:n.-105-4745T>A
NM_032049.4:c.-262-4745T>A NP_114438.3:n.-262-4745T>A