Canonical Allele Identifier: CA414339419
Gene: AGTR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173200G>C , CM000685.2:g.116173200G>C GRCh38
NC_000023.10:g.115304453G>C , CM000685.1:g.115304453G>C GRCh37
NC_000023.9:g.115218481G>C NCBI36
NG_016326.1:g.7496G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.920G>C MANE Select ENSP00000360973.4:p.Gly307Ala
ENST00000680409.1:n.1388G>C
ENST00000681852.1:c.920G>C ENSP00000505750.1:p.Gly307Ala
ENST00000371906.4:c.920G>C ENSP00000360973.4:p.Gly307Ala
NM_000686.4:c.920G>C NP_000677.2:p.Gly307Ala
XM_011537533.1:c.920G>C XP_011535835.1:p.Gly307Ala
NM_000686.5:c.920G>C MANE Select NP_000677.2:p.Gly307Ala
NM_001385624.1:c.920G>C NP_001372553.1:p.Gly307Ala