Canonical Allele Identifier: CA1401209461
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530981G= , CM000665.2:g.129530981G= GRCh38
NC_000003.11:g.129249824G= , CM000665.1:g.129249824G= GRCh37
NC_000003.10:g.130732514G= NCBI36
NG_009115.1:g.7343G=

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.467G= MANE Select ENSP00000296271.3:p.Gly156=
ENST00000296271.3:c.467G= ENSP00000296271.3:p.Gly156=
NM_000539.3:c.467G= MANE Select NP_000530.1:p.Gly156=