Canonical Allele Identifier: CA85566052

Gene: AGTR1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.148717966T>C , CM000665.2:g.148717966T>C	GRCh38
NC_000003.11:g.148435753T>C , CM000665.1:g.148435753T>C	GRCh37
NC_000003.10:g.149918443T>C	NCBI36
NG_008468.1:g.25096T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349243.8:c.-48+9939T>C MANE Select	ENSP00000273430.3:n.-48+9939T>C
ENST00000418473.7:c.-105-12214T>C	ENSP00000398832.4:n.-105-12214T>C
ENST00000349243.7:c.-48+9939T>C	ENSP00000273430.3:n.-48+9939T>C
ENST00000404754.2:c.-48+19817T>C	ENSP00000385612.2:n.-48+19817T>C
ENST00000475166.5:n.216+9939T>C
ENST00000497524.5:c.-48+19839T>C	ENSP00000419422.1:n.-48+19839T>C
NM_000685.4:c.-48+9939T>C	NP_000676.1:n.-48+9939T>C
NM_004835.4:c.1-12214T>C	NP_004826.5:n.1-12214T>C
NM_009585.3:c.-48+19839T>C	NP_033611.1:n.-48+19839T>C
NM_031850.3:c.-1+9939T>C	NP_114038.4:n.-1+9939T>C
NM_000685.5:c.-48+9939T>C MANE Select	NP_000676.1:n.-48+9939T>C
NM_001382736.1:c.-48+19817T>C	NP_001369665.1:n.-48+19817T>C
NM_001382737.1:c.-48+9939T>C	NP_001369666.1:n.-48+9939T>C
NM_004835.5:c.-105-12214T>C	NP_004826.6:n.-105-12214T>C
NM_009585.4:c.-48+19839T>C	NP_033611.1:n.-48+19839T>C
NM_031850.4:c.-106+9939T>C	NP_114038.5:n.-106+9939T>C
NM_032049.4:c.-262-12214T>C	NP_114438.3:n.-262-12214T>C