Canonical Allele Identifier: CA414337820
Gene: AGTR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172485T>A , CM000685.2:g.116172485T>A GRCh38
NC_000023.10:g.115303738T>A , CM000685.1:g.115303738T>A GRCh37
NC_000023.9:g.115217766T>A NCBI36
NG_016326.1:g.6781T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.205T>A MANE Select ENSP00000360973.4:p.Phe69Ile
ENST00000680409.1:n.673T>A
ENST00000681852.1:c.205T>A ENSP00000505750.1:p.Phe69Ile
ENST00000371906.4:c.205T>A ENSP00000360973.4:p.Phe69Ile
NM_000686.4:c.205T>A NP_000677.2:p.Phe69Ile
XM_011537533.1:c.205T>A XP_011535835.1:p.Phe69Ile
NM_000686.5:c.205T>A MANE Select NP_000677.2:p.Phe69Ile
NM_001385624.1:c.205T>A NP_001372553.1:p.Phe69Ile