Canonical Allele Identifier: CA2667614661
Gene: RHO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528710_129528720del , CM000665.2:g.129528710_129528720del GRCh38
NC_000003.11:g.129247553_129247563del , CM000665.1:g.129247553_129247563del GRCh37
NC_000003.10:g.130730243_130730253del NCBI36
NG_009115.1:g.5072_5082del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.-24_-14del MANE Select ENSP00000296271.3:n.-24_-14del
ENST00000296271.3:c.-24_-14del ENSP00000296271.3:n.-24_-14del
NM_000539.3:c.-24_-14del MANE Select NP_000530.1:n.-24_-14del