Canonical Allele Identifier: CA2453331766
Gene: AGTR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172621C= , CM000685.2:g.116172621C= GRCh38
NC_000023.10:g.115303874C= , CM000685.1:g.115303874C= GRCh37
NC_000023.9:g.115217902C= NCBI36
NG_016326.1:g.6917C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.341C= MANE Select ENSP00000360973.4:p.Pro114=
ENST00000680409.1:n.809C=
ENST00000681852.1:c.341C= ENSP00000505750.1:p.Pro114=
ENST00000371906.4:c.341C= ENSP00000360973.4:p.Pro114=
NM_000686.4:c.341C= NP_000677.2:p.Pro114=
XM_011537533.1:c.341C= XP_011535835.1:p.Pro114=
NM_000686.5:c.341C= MANE Select NP_000677.2:p.Pro114=
NM_001385624.1:c.341C= NP_001372553.1:p.Pro114=