Canonical Allele Identifier: CA2453331559
Gene: AGTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1922464203

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172007del , CM000685.2:g.116172007del GRCh38
NC_000023.10:g.115303260del , CM000685.1:g.115303260del GRCh37
NC_000023.9:g.115217288del NCBI36
NG_016326.1:g.6303del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.-35-239del MANE Select ENSP00000360973.4:n.-35-239del
ENST00000680409.1:n.195del
ENST00000681852.1:c.-35-239del ENSP00000505750.1:n.-35-239del
ENST00000371906.4:c.-35-239del ENSP00000360973.4:n.-35-239del
NM_000686.4:c.-35-239del NP_000677.2:n.-35-239del
XM_011537533.1:c.-35-239del XP_011535835.1:n.-35-239del
NM_000686.5:c.-35-239del MANE Select NP_000677.2:n.-35-239del
NM_001385624.1:c.-35-239del NP_001372553.1:n.-35-239del