Canonical Allele Identifier: CA2694510935
Gene: AGTR2 HGNC NCBI

Linked Data

gnomAD v4: X-116173537-GC-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173540del , CM000685.2:g.116173540del GRCh38
NC_000023.10:g.115304793del , CM000685.1:g.115304793del GRCh37
NC_000023.9:g.115218821del NCBI36
NG_016326.1:g.7836del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.*168del MANE Select ENSP00000360973.4:n.*168del
ENST00000371906.4:c.*168del ENSP00000360973.4:n.*168del
NM_000686.4:c.*168del NP_000677.2:n.*168del
XM_011537533.1:c.*168del XP_011535835.1:n.*168del
NM_000686.5:c.*168del MANE Select NP_000677.2:n.*168del
NM_001385624.1:c.*168del NP_001372553.1:n.*168del
Search 100 bp 5'
Search 100 bp 3'