Canonical Allele Identifier: CA2453332057
Gene: AGTR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173548T= , CM000685.2:g.116173548T= GRCh38
NC_000023.10:g.115304801T= , CM000685.1:g.115304801T= GRCh37
NC_000023.9:g.115218829T= NCBI36
NG_016326.1:g.7844T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.*176T= MANE Select ENSP00000360973.4:n.*176T=
ENST00000371906.4:c.*176T= ENSP00000360973.4:n.*176T=
NM_000686.4:c.*176T= NP_000677.2:n.*176T=
XM_011537533.1:c.*176T= XP_011535835.1:n.*176T=
NM_000686.5:c.*176T= MANE Select NP_000677.2:n.*176T=
NM_001385624.1:c.*176T= NP_001372553.1:n.*176T=