Canonical Allele Identifier: CA2704006593
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2108749081
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528688_129528690del , CM000665.2:g.129528688_129528690del GRCh38
NC_000003.11:g.129247531_129247533del , CM000665.1:g.129247531_129247533del GRCh37
NC_000003.10:g.130730221_130730223del NCBI36
NG_009115.1:g.5050_5052del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.-46_-44del MANE Select ENSP00000296271.3:n.-46_-44del
ENST00000296271.3:c.-46_-44del ENSP00000296271.3:n.-46_-44del
NM_000539.3:c.-46_-44del MANE Select NP_000530.1:n.-46_-44del
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