Canonical Allele Identifier: CA1401209452
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530977A= , CM000665.2:g.129530977A= GRCh38
NC_000003.11:g.129249820A= , CM000665.1:g.129249820A= GRCh37
NC_000003.10:g.130732510A= NCBI36
NG_009115.1:g.7339A=

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.463A= MANE Select ENSP00000296271.3:p.Met155=
ENST00000296271.3:c.463A= ENSP00000296271.3:p.Met155=
NM_000539.3:c.463A= MANE Select NP_000530.1:p.Met155=