Canonical Allele Identifier: CA414337827
Gene: AGTR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172487T>G , CM000685.2:g.116172487T>G GRCh38
NC_000023.10:g.115303740T>G , CM000685.1:g.115303740T>G GRCh37
NC_000023.9:g.115217768T>G NCBI36
NG_016326.1:g.6783T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.207T>G MANE Select ENSP00000360973.4:p.Phe69Leu
ENST00000680409.1:n.675T>G
ENST00000681852.1:c.207T>G ENSP00000505750.1:p.Phe69Leu
ENST00000371906.4:c.207T>G ENSP00000360973.4:p.Phe69Leu
NM_000686.4:c.207T>G NP_000677.2:p.Phe69Leu
XM_011537533.1:c.207T>G XP_011535835.1:p.Phe69Leu
NM_000686.5:c.207T>G MANE Select NP_000677.2:p.Phe69Leu
NM_001385624.1:c.207T>G NP_001372553.1:p.Phe69Leu