Canonical Allele Identifier: CA2758363804
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529234_129529240del , CM000665.2:g.129529234_129529240del GRCh38
NC_000003.11:g.129248077_129248083del , CM000665.1:g.129248077_129248083del GRCh37
NC_000003.10:g.130730767_130730773del NCBI36
NG_009115.1:g.5596_5602del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+140_361+146del MANE Select ENSP00000296271.3:n.361+140_361+146del
ENST00000296271.3:c.361+140_361+146del ENSP00000296271.3:n.361+140_361+146del
NM_000539.3:c.361+140_361+146del MANE Select NP_000530.1:n.361+140_361+146del