Canonical Allele Identifier: CA2823125673
Gene: AGTR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173583_116173584insAG , CM000685.2:g.116173583_116173584insAG GRCh38
NC_000023.10:g.115304836_115304837insAG , CM000685.1:g.115304836_115304837insAG GRCh37
NC_000023.9:g.115218864_115218865insAG NCBI36
NG_016326.1:g.7879_7880insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.*211_*212insAG MANE Select ENSP00000360973.4:n.*211_*212insAG
ENST00000371906.4:c.*211_*212insAG ENSP00000360973.4:n.*211_*212insAG
NM_000686.4:c.*211_*212insAG NP_000677.2:n.*211_*212insAG
XM_011537533.1:c.*211_*212insAG XP_011535835.1:n.*211_*212insAG
NM_000686.5:c.*211_*212insAG MANE Select NP_000677.2:n.*211_*212insAG
NM_001385624.1:c.*211_*212insAG NP_001372553.1:n.*211_*212insAG