Canonical Allele Identifier: CA2694511005
Gene: AGTR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173599_116173600del , CM000685.2:g.116173599_116173600del GRCh38
NC_000023.10:g.115304852_115304853del , CM000685.1:g.115304852_115304853del GRCh37
NC_000023.9:g.115218880_115218881del NCBI36
NG_016326.1:g.7895_7896del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.*227_*228del MANE Select ENSP00000360973.4:n.*227_*228del
ENST00000371906.4:c.*227_*228del ENSP00000360973.4:n.*227_*228del
NM_000686.4:c.*227_*228del NP_000677.2:n.*227_*228del
XM_011537533.1:c.*227_*228del XP_011535835.1:n.*227_*228del
NM_000686.5:c.*227_*228del MANE Select NP_000677.2:n.*227_*228del
NM_001385624.1:c.*227_*228del NP_001372553.1:n.*227_*228del