Canonical Allele Identifier: CA2758363813
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529251_129529252del , CM000665.2:g.129529251_129529252del GRCh38
NC_000003.11:g.129248094_129248095del , CM000665.1:g.129248094_129248095del GRCh37
NC_000003.10:g.130730784_130730785del NCBI36
NG_009115.1:g.5613_5614del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+157_361+158del MANE Select ENSP00000296271.3:n.361+157_361+158del
ENST00000296271.3:c.361+157_361+158del ENSP00000296271.3:n.361+157_361+158del
NM_000539.3:c.361+157_361+158del MANE Select NP_000530.1:n.361+157_361+158del