Canonical Allele Identifier: CA2453331973
Gene: AGTR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173268C= , CM000685.2:g.116173268C= GRCh38
NC_000023.10:g.115304521C= , CM000685.1:g.115304521C= GRCh37
NC_000023.9:g.115218549C= NCBI36
NG_016326.1:g.7564C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.988C= MANE Select ENSP00000360973.4:p.Arg330=
ENST00000680409.1:n.1456C=
ENST00000681852.1:c.988C= ENSP00000505750.1:p.Arg330=
ENST00000371906.4:c.988C= ENSP00000360973.4:p.Arg330=
NM_000686.4:c.988C= NP_000677.2:p.Arg330=
XM_011537533.1:c.988C= XP_011535835.1:p.Arg330=
NM_000686.5:c.988C= MANE Select NP_000677.2:p.Arg330=
NM_001385624.1:c.988C= NP_001372553.1:p.Arg330=