Canonical Allele Identifier: CA2453332004
Gene: AGTR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173364G= , CM000685.2:g.116173364G= GRCh38
NC_000023.10:g.115304617G= , CM000685.1:g.115304617G= GRCh37
NC_000023.9:g.115218645G= NCBI36
NG_016326.1:g.7660G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.1084G= MANE Select ENSP00000360973.4:p.Val362=
ENST00000680409.1:n.1552G=
ENST00000681852.1:c.1084G= ENSP00000505750.1:p.Val362=
ENST00000371906.4:c.1084G= ENSP00000360973.4:p.Val362=
NM_000686.4:c.1084G= NP_000677.2:p.Val362=
XM_011537533.1:c.1084G= XP_011535835.1:p.Val362=
NM_000686.5:c.1084G= MANE Select NP_000677.2:p.Val362=
NM_001385624.1:c.1084G= NP_001372553.1:p.Val362=