Canonical Allele Identifier: CA2453331600
Gene: AGTR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172148_116172149delinsCT , CM000685.2:g.116172148_116172149delinsCT GRCh38
NC_000023.10:g.115303401_115303402delinsCT , CM000685.1:g.115303401_115303402delinsCT GRCh37
NC_000023.9:g.115217429_115217430delinsCT NCBI36
NG_016326.1:g.6444_6445delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.-35-98_-35-97delinsCT MANE Select ENSP00000360973.4:n.-35-98_-35-97delinsCT
ENST00000680409.1:n.336_337delinsCT
ENST00000681852.1:c.-35-98_-35-97delinsCT ENSP00000505750.1:n.-35-98_-35-97delinsCT
ENST00000371906.4:c.-35-98_-35-97delinsCT ENSP00000360973.4:n.-35-98_-35-97delinsCT
NM_000686.4:c.-35-98_-35-97delinsCT NP_000677.2:n.-35-98_-35-97delinsCT
XM_011537533.1:c.-35-98_-35-97delinsCT XP_011535835.1:n.-35-98_-35-97delinsCT
NM_000686.5:c.-35-98_-35-97delinsCT MANE Select NP_000677.2:n.-35-98_-35-97delinsCT
NM_001385624.1:c.-35-98_-35-97delinsCT NP_001372553.1:n.-35-98_-35-97delinsCT