Canonical Allele Identifier: CA2453331741
Gene: AGTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1922488734
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172543_116172548del , CM000685.2:g.116172543_116172548del GRCh38
NC_000023.10:g.115303796_115303801del , CM000685.1:g.115303796_115303801del GRCh37
NC_000023.9:g.115217824_115217829del NCBI36
NG_016326.1:g.6839_6844del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.263_268del MANE Select ENSP00000360973.4:p.Val88_Ala89del
ENST00000680409.1:n.731_736del
ENST00000681852.1:c.263_268del ENSP00000505750.1:p.Val88_Ala89del
ENST00000371906.4:c.263_268del ENSP00000360973.4:p.Val88_Ala89del
NM_000686.4:c.263_268del NP_000677.2:p.Val88_Ala89del
XM_011537533.1:c.263_268del XP_011535835.1:p.Val88_Ala89del
NM_000686.5:c.263_268del MANE Select NP_000677.2:p.Val88_Ala89del
NM_001385624.1:c.263_268del NP_001372553.1:p.Val88_Ala89del
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