Canonical Allele Identifier: CA1136568734

Gene: AGTR2

Linked Data

• dbSNP Id: rs1922464842
• gnomAD v3: X-116172042-C-CT
• gnomAD v4: X-116172042-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.116172048dup , CM000685.2:g.116172048dup	GRCh38
NC_000023.10:g.115303301dup , CM000685.1:g.115303301dup	GRCh37
NC_000023.9:g.115217329dup	NCBI36
NG_016326.1:g.6344dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371906.5:c.-35-198dup MANE Select	ENSP00000360973.4:n.-35-198dup
ENST00000680409.1:n.236dup
ENST00000681852.1:c.-35-198dup	ENSP00000505750.1:n.-35-198dup
ENST00000371906.4:c.-35-198dup	ENSP00000360973.4:n.-35-198dup
NM_000686.4:c.-35-198dup	NP_000677.2:n.-35-198dup
XM_011537533.1:c.-35-198dup	XP_011535835.1:n.-35-198dup
NM_000686.5:c.-35-198dup MANE Select	NP_000677.2:n.-35-198dup
NM_001385624.1:c.-35-198dup	NP_001372553.1:n.-35-198dup