Canonical Allele Identifier: CA2823125642
Gene: AGTR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172145_116172146del , CM000685.2:g.116172145_116172146del GRCh38
NC_000023.10:g.115303398_115303399del , CM000685.1:g.115303398_115303399del GRCh37
NC_000023.9:g.115217426_115217427del NCBI36
NG_016326.1:g.6441_6442del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.-35-101_-35-100del MANE Select ENSP00000360973.4:n.-35-101_-35-100del
ENST00000680409.1:n.333_334del
ENST00000681852.1:c.-35-101_-35-100del ENSP00000505750.1:n.-35-101_-35-100del
ENST00000371906.4:c.-35-101_-35-100del ENSP00000360973.4:n.-35-101_-35-100del
NM_000686.4:c.-35-101_-35-100del NP_000677.2:n.-35-101_-35-100del
XM_011537533.1:c.-35-101_-35-100del XP_011535835.1:n.-35-101_-35-100del
NM_000686.5:c.-35-101_-35-100del MANE Select NP_000677.2:n.-35-101_-35-100del
NM_001385624.1:c.-35-101_-35-100del NP_001372553.1:n.-35-101_-35-100del