Canonical Allele Identifier: CA1401213256
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129533655G= , CM000665.2:g.129533655G= GRCh38
NC_000003.11:g.129252498G= , CM000665.1:g.129252498G= GRCh37
NC_000003.10:g.130735188G= NCBI36
NG_009115.1:g.10017G=

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.984G= MANE Select ENSP00000296271.3:p.Leu328=
ENST00000296271.3:c.984G= ENSP00000296271.3:p.Leu328=
NM_000539.3:c.984G= MANE Select NP_000530.1:p.Leu328=