Canonical Allele Identifier: CA354497836

Gene: RHO

Linked Data

• MyVariant Identifiers: chr3:g.129249721G>C (hg19) ; chr3:g.129530878G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129530878G>C , CM000665.2:g.129530878G>C	GRCh38
NC_000003.11:g.129249721G>C , CM000665.1:g.129249721G>C	GRCh37
NC_000003.10:g.130732411G>C	NCBI36
NG_009115.1:g.7240G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000296271.4:c.364G>C MANE Select	ENSP00000296271.3:p.Glu122Gln
ENST00000296271.3:c.364G>C	ENSP00000296271.3:p.Glu122Gln
NM_000539.3:c.364G>C MANE Select	NP_000530.1:p.Glu122Gln