Canonical Allele Identifier: CA2577961832

Gene: RHO

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129533556C>G , CM000665.2:g.129533556C>G	GRCh38
NC_000003.11:g.129252399C>G , CM000665.1:g.129252399C>G	GRCh37
NC_000003.10:g.130735089C>G	NCBI36
NG_009115.1:g.9918C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000296271.4:c.937-52C>G MANE Select	ENSP00000296271.3:n.937-52C>G
ENST00000296271.3:c.937-52C>G	ENSP00000296271.3:n.937-52C>G
NM_000539.3:c.937-52C>G MANE Select	NP_000530.1:n.937-52C>G