Canonical Allele Identifier: CA2823125661
Gene: AGTR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173450_116173451insCC , CM000685.2:g.116173450_116173451insCC GRCh38
NC_000023.10:g.115304703_115304704insCC , CM000685.1:g.115304703_115304704insCC GRCh37
NC_000023.9:g.115218731_115218732insCC NCBI36
NG_016326.1:g.7746_7747insCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.*78_*79insCC MANE Select ENSP00000360973.4:n.*78_*79insCC
ENST00000371906.4:c.*78_*79insCC ENSP00000360973.4:n.*78_*79insCC
NM_000686.4:c.*78_*79insCC NP_000677.2:n.*78_*79insCC
XM_011537533.1:c.*78_*79insCC XP_011535835.1:n.*78_*79insCC
NM_000686.5:c.*78_*79insCC MANE Select NP_000677.2:n.*78_*79insCC
NM_001385624.1:c.*78_*79insCC NP_001372553.1:n.*78_*79insCC