Canonical Allele Identifier: CA2453331594

Gene: AGTR2

Linked Data

• dbSNP Id: rs1922467828
• gnomAD v4: X-116172138-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.116172138T>C , CM000685.2:g.116172138T>C	GRCh38
NC_000023.10:g.115303391T>C , CM000685.1:g.115303391T>C	GRCh37
NC_000023.9:g.115217419T>C	NCBI36
NG_016326.1:g.6434T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371906.5:c.-35-108T>C MANE Select	ENSP00000360973.4:n.-35-108T>C
ENST00000680409.1:n.326T>C
ENST00000681852.1:c.-35-108T>C	ENSP00000505750.1:n.-35-108T>C
ENST00000371906.4:c.-35-108T>C	ENSP00000360973.4:n.-35-108T>C
NM_000686.4:c.-35-108T>C	NP_000677.2:n.-35-108T>C
XM_011537533.1:c.-35-108T>C	XP_011535835.1:n.-35-108T>C
NM_000686.5:c.-35-108T>C MANE Select	NP_000677.2:n.-35-108T>C
NM_001385624.1:c.-35-108T>C	NP_001372553.1:n.-35-108T>C