Canonical Allele Identifier: CA1401208930
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530571A= , CM000665.2:g.129530571A= GRCh38
NC_000003.11:g.129249414A= , CM000665.1:g.129249414A= GRCh37
NC_000003.10:g.130732104A= NCBI36
NG_009115.1:g.6933A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-305A= MANE Select ENSP00000296271.3:n.362-305A=
ENST00000296271.3:c.362-305A= ENSP00000296271.3:n.362-305A=
NM_000539.3:c.362-305A= MANE Select NP_000530.1:n.362-305A=