Canonical Allele Identifier: CA2694510807

Gene: AGTR2

Linked Data

• gnomAD v4: X-116172148-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.116172156_116172157del , CM000685.2:g.116172156_116172157del	GRCh38
NC_000023.10:g.115303409_115303410del , CM000685.1:g.115303409_115303410del	GRCh37
NC_000023.9:g.115217437_115217438del	NCBI36
NG_016326.1:g.6452_6453del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371906.5:c.-35-90_-35-89del MANE Select	ENSP00000360973.4:n.-35-90_-35-89del
ENST00000680409.1:n.344_345del
ENST00000681852.1:c.-35-90_-35-89del	ENSP00000505750.1:n.-35-90_-35-89del
ENST00000371906.4:c.-35-90_-35-89del	ENSP00000360973.4:n.-35-90_-35-89del
NM_000686.4:c.-35-90_-35-89del	NP_000677.2:n.-35-90_-35-89del
XM_011537533.1:c.-35-90_-35-89del	XP_011535835.1:n.-35-90_-35-89del
NM_000686.5:c.-35-90_-35-89del MANE Select	NP_000677.2:n.-35-90_-35-89del
NM_001385624.1:c.-35-90_-35-89del	NP_001372553.1:n.-35-90_-35-89del