Canonical Allele Identifier: CA1401205713
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528962C= , CM000665.2:g.129528962C= GRCh38
NC_000003.11:g.129247805C= , CM000665.1:g.129247805C= GRCh37
NC_000003.10:g.130730495C= NCBI36
NG_009115.1:g.5324C=

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.229C= MANE Select ENSP00000296271.3:p.Leu77=
ENST00000296271.3:c.229C= ENSP00000296271.3:p.Leu77=
NM_000539.3:c.229C= MANE Select NP_000530.1:p.Leu77=