Canonical Allele Identifier: CA151691
Gene: AGTR2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 11716
dbSNP Id: rs121917810

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172342G>T , CM000685.2:g.116172342G>T GRCh38
NC_000023.9:g.115217623G>T NCBI36
NC_000023.10:g.115303595G>T , CM000685.1:g.115303595G>T GRCh37
NG_016326.1:g.6638G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371906.4:c.62G>T ENSP00000360973.4:p.Gly21Val
NM_000686.4:c.62G>T VV NP_000677.2:p.Gly21Val
XM_011537533.1:c.62G>T XP_011535835.1:p.Gly21Val