Canonical Allele Identifier: CA85562154
Gene: AGTR1 HGNC NCBI

Linked Data

dbSNP Id: rs1013717840

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.148708699C>T , CM000665.2:g.148708699C>T GRCh38
NC_000003.11:g.148426486C>T , CM000665.1:g.148426486C>T GRCh37
NC_000003.10:g.149909176C>T NCBI36
NG_008468.1:g.15829C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000349243.8:c.-48+672C>T MANE Select ENSP00000273430.3:n.-48+672C>T
ENST00000418473.7:c.-106+10572C>T ENSP00000398832.4:n.-106+10572C>T
ENST00000349243.7:c.-48+672C>T ENSP00000273430.3:n.-48+672C>T
ENST00000404754.2:c.-48+10550C>T ENSP00000385612.2:n.-48+10550C>T
ENST00000475166.5:n.216+672C>T
ENST00000497524.5:c.-48+10572C>T ENSP00000419422.1:n.-48+10572C>T
NM_000685.4:c.-48+672C>T NP_000676.1:n.-48+672C>T
NM_004835.4:c.-1+10572C>T NP_004826.5:n.-1+10572C>T
NM_009585.3:c.-48+10572C>T NP_033611.1:n.-48+10572C>T
NM_031850.3:c.-1+672C>T NP_114038.4:n.-1+672C>T
NM_000685.5:c.-48+672C>T MANE Select NP_000676.1:n.-48+672C>T
NM_001382736.1:c.-48+10550C>T NP_001369665.1:n.-48+10550C>T
NM_001382737.1:c.-48+672C>T NP_001369666.1:n.-48+672C>T
NM_004835.5:c.-106+10572C>T NP_004826.6:n.-106+10572C>T
NM_009585.4:c.-48+10572C>T NP_033611.1:n.-48+10572C>T
NM_031850.4:c.-106+672C>T NP_114038.5:n.-106+672C>T
NM_032049.4:c.-263+10572C>T NP_114438.3:n.-263+10572C>T