Canonical Allele Identifier: CA414339668
Gene: AGTR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173311G>T , CM000685.2:g.116173311G>T GRCh38
NC_000023.10:g.115304564G>T , CM000685.1:g.115304564G>T GRCh37
NC_000023.9:g.115218592G>T NCBI36
NG_016326.1:g.7607G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.1031G>T MANE Select ENSP00000360973.4:p.Arg344Ile
ENST00000680409.1:n.1499G>T
ENST00000681852.1:c.1031G>T ENSP00000505750.1:p.Arg344Ile
ENST00000371906.4:c.1031G>T ENSP00000360973.4:p.Arg344Ile
NM_000686.4:c.1031G>T NP_000677.2:p.Arg344Ile
XM_011537533.1:c.1031G>T XP_011535835.1:p.Arg344Ile
NM_000686.5:c.1031G>T MANE Select NP_000677.2:p.Arg344Ile
NM_001385624.1:c.1031G>T NP_001372553.1:p.Arg344Ile