Canonical Allele Identifier: CA414338116
Gene: AGTR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172616T>G , CM000685.2:g.116172616T>G GRCh38
NC_000023.10:g.115303869T>G , CM000685.1:g.115303869T>G GRCh37
NC_000023.9:g.115217897T>G NCBI36
NG_016326.1:g.6912T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.336T>G MANE Select ENSP00000360973.4:p.Phe112Leu
ENST00000680409.1:n.804T>G
ENST00000681852.1:c.336T>G ENSP00000505750.1:p.Phe112Leu
ENST00000371906.4:c.336T>G ENSP00000360973.4:p.Phe112Leu
NM_000686.4:c.336T>G NP_000677.2:p.Phe112Leu
XM_011537533.1:c.336T>G XP_011535835.1:p.Phe112Leu
NM_000686.5:c.336T>G MANE Select NP_000677.2:p.Phe112Leu
NM_001385624.1:c.336T>G NP_001372553.1:p.Phe112Leu