Canonical Allele Identifier: CA414339699
Gene: AGTR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173323C>A , CM000685.2:g.116173323C>A GRCh38
NC_000023.10:g.115304576C>A , CM000685.1:g.115304576C>A GRCh37
NC_000023.9:g.115218604C>A NCBI36
NG_016326.1:g.7619C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.1043C>A MANE Select ENSP00000360973.4:p.Ser348Tyr
ENST00000680409.1:n.1511C>A
ENST00000681852.1:c.1043C>A ENSP00000505750.1:p.Ser348Tyr
ENST00000371906.4:c.1043C>A ENSP00000360973.4:p.Ser348Tyr
NM_000686.4:c.1043C>A NP_000677.2:p.Ser348Tyr
XM_011537533.1:c.1043C>A XP_011535835.1:p.Ser348Tyr
NM_000686.5:c.1043C>A MANE Select NP_000677.2:p.Ser348Tyr
NM_001385624.1:c.1043C>A NP_001372553.1:p.Ser348Tyr