Canonical Allele Identifier: CA1401209093
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530798C= , CM000665.2:g.129530798C= GRCh38
NC_000003.11:g.129249641C= , CM000665.1:g.129249641C= GRCh37
NC_000003.10:g.130732331C= NCBI36
NG_009115.1:g.7160C=

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.362-78C= MANE Select ENSP00000296271.3:n.362-78C=
ENST00000296271.3:c.362-78C= ENSP00000296271.3:n.362-78C=
NM_000539.3:c.362-78C= MANE Select NP_000530.1:n.362-78C=