Canonical Allele Identifier: CA1401206587
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529242C= , CM000665.2:g.129529242C= GRCh38
NC_000003.11:g.129248085C= , CM000665.1:g.129248085C= GRCh37
NC_000003.10:g.130730775C= NCBI36
NG_009115.1:g.5604C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+148C= MANE Select ENSP00000296271.3:n.361+148C=
ENST00000296271.3:c.361+148C= ENSP00000296271.3:n.361+148C=
NM_000539.3:c.361+148C= MANE Select NP_000530.1:n.361+148C=