Canonical Allele Identifier: CA2453331961
Gene: AGTR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173229C= , CM000685.2:g.116173229C= GRCh38
NC_000023.10:g.115304482C= , CM000685.1:g.115304482C= GRCh37
NC_000023.9:g.115218510C= NCBI36
NG_016326.1:g.7525C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.949C= MANE Select ENSP00000360973.4:p.Leu317=
ENST00000680409.1:n.1417C=
ENST00000681852.1:c.949C= ENSP00000505750.1:p.Leu317=
ENST00000371906.4:c.949C= ENSP00000360973.4:p.Leu317=
NM_000686.4:c.949C= NP_000677.2:p.Leu317=
XM_011537533.1:c.949C= XP_011535835.1:p.Leu317=
NM_000686.5:c.949C= MANE Select NP_000677.2:p.Leu317=
NM_001385624.1:c.949C= NP_001372553.1:p.Leu317=