Canonical Allele Identifier: CA2453332048
Gene: AGTR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173523G= , CM000685.2:g.116173523G= GRCh38
NC_000023.10:g.115304776G= , CM000685.1:g.115304776G= GRCh37
NC_000023.9:g.115218804G= NCBI36
NG_016326.1:g.7819G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.*151G= MANE Select ENSP00000360973.4:n.*151G=
ENST00000371906.4:c.*151G= ENSP00000360973.4:n.*151G=
NM_000686.4:c.*151G= NP_000677.2:n.*151G=
XM_011537533.1:c.*151G= XP_011535835.1:n.*151G=
NM_000686.5:c.*151G= MANE Select NP_000677.2:n.*151G=
NM_001385624.1:c.*151G= NP_001372553.1:n.*151G=