Canonical Allele Identifier: CA2453331589
Gene: AGTR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172123T= , CM000685.2:g.116172123T= GRCh38
NC_000023.10:g.115303376T= , CM000685.1:g.115303376T= GRCh37
NC_000023.9:g.115217404T= NCBI36
NG_016326.1:g.6419T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.-35-123T= MANE Select ENSP00000360973.4:n.-35-123T=
ENST00000680409.1:n.311T=
ENST00000681852.1:c.-35-123T= ENSP00000505750.1:n.-35-123T=
ENST00000371906.4:c.-35-123T= ENSP00000360973.4:n.-35-123T=
NM_000686.4:c.-35-123T= NP_000677.2:n.-35-123T=
XM_011537533.1:c.-35-123T= XP_011535835.1:n.-35-123T=
NM_000686.5:c.-35-123T= MANE Select NP_000677.2:n.-35-123T=
NM_001385624.1:c.-35-123T= NP_001372553.1:n.-35-123T=