Canonical Allele Identifier: CA2758363842
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529328_129529341del , CM000665.2:g.129529328_129529341del GRCh38
NC_000003.11:g.129248171_129248184del , CM000665.1:g.129248171_129248184del GRCh37
NC_000003.10:g.130730861_130730874del NCBI36
NG_009115.1:g.5690_5703del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+234_361+247del MANE Select ENSP00000296271.3:n.361+234_361+247del
ENST00000296271.3:c.361+234_361+247del ENSP00000296271.3:n.361+234_361+247del
NM_000539.3:c.361+234_361+247del MANE Select NP_000530.1:n.361+234_361+247del