Canonical Allele Identifier: CA2758363912
Gene: RHO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530775_129530806del , CM000665.2:g.129530775_129530806del GRCh38
NC_000003.11:g.129249618_129249649del , CM000665.1:g.129249618_129249649del GRCh37
NC_000003.10:g.130732308_130732339del NCBI36
NG_009115.1:g.7137_7168del

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.362-101_362-70del MANE Select ENSP00000296271.3:n.362-101_362-70del
ENST00000296271.3:c.362-101_362-70del ENSP00000296271.3:n.362-101_362-70del
NM_000539.3:c.362-101_362-70del MANE Select NP_000530.1:n.362-101_362-70del
Search 100 bp 5'
Search 100 bp 3'