Canonical Allele Identifier: CA1136568739

Gene: AGTR2

Linked Data

• dbSNP Id: rs1922467132
• gnomAD v3: X-116172115-GCT-G
• gnomAD v4: X-116172115-GCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.116172118_116172119del , CM000685.2:g.116172118_116172119del	GRCh38
NC_000023.10:g.115303371_115303372del , CM000685.1:g.115303371_115303372del	GRCh37
NC_000023.9:g.115217399_115217400del	NCBI36
NG_016326.1:g.6414_6415del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371906.5:c.-35-128_-35-127del MANE Select	ENSP00000360973.4:n.-35-128_-35-127del
ENST00000680409.1:n.306_307del
ENST00000681852.1:c.-35-128_-35-127del	ENSP00000505750.1:n.-35-128_-35-127del
ENST00000371906.4:c.-35-128_-35-127del	ENSP00000360973.4:n.-35-128_-35-127del
NM_000686.4:c.-35-128_-35-127del	NP_000677.2:n.-35-128_-35-127del
XM_011537533.1:c.-35-128_-35-127del	XP_011535835.1:n.-35-128_-35-127del
NM_000686.5:c.-35-128_-35-127del MANE Select	NP_000677.2:n.-35-128_-35-127del
NM_001385624.1:c.-35-128_-35-127del	NP_001372553.1:n.-35-128_-35-127del