Canonical Allele Identifier: CA354470163

Gene: RHO

Linked Data

• MyVariant Identifiers: chr3:g.129251374A>C (hg19) ; chr3:g.129532531A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129532531A>C , CM000665.2:g.129532531A>C	GRCh38
NC_000003.11:g.129251374A>C , CM000665.1:g.129251374A>C	GRCh37
NC_000003.10:g.130734064A>C	NCBI36
NG_009115.1:g.8893A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000296271.4:c.697-2A>C MANE Select	ENSP00000296271.3:n.697-2A>C
ENST00000296271.3:c.697-2A>C	ENSP00000296271.3:n.697-2A>C
NM_000539.3:c.697-2A>C MANE Select	NP_000530.1:n.697-2A>C