Canonical Allele Identifier: CA82648160
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs570795323

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530566_129530567insAACACACACACACACACA , CM000665.2:g.129530566_129530567insAACACACACACACACACA GRCh38
NC_000003.11:g.129249409_129249410insAACACACACACACACACA , CM000665.1:g.129249409_129249410insAACACACACACACACACA GRCh37
NC_000003.10:g.130732099_130732100insAACACACACACACACACA NCBI36
NG_009115.1:g.6928_6929insAACACACACACACACACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-310_362-309insAACACACACACACACACA MANE Select ENSP00000296271.3:n.362-310_362-309insAACACACACACACACACA
ENST00000296271.3:c.362-310_362-309insAACACACACACACACACA ENSP00000296271.3:n.362-310_362-309insAACACACACACACACACA
NM_000539.3:c.362-310_362-309insAACACACACACACACACA MANE Select NP_000530.1:n.362-310_362-309insAACACACACACACACACA