Canonical Allele Identifier: CA546417611

Gene: RHO

Linked Data

• dbSNP Id: rs1429888921
• gnomAD v2: 3-129247984-A-C
• gnomAD v4: 3-129529141-A-C
• MyVariant Identifiers: chr3:g.129247984A>C (hg19) ; chr3:g.129529141A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129529141A>C , CM000665.2:g.129529141A>C	GRCh38
NC_000003.11:g.129247984A>C , CM000665.1:g.129247984A>C	GRCh37
NC_000003.10:g.130730674A>C	NCBI36
NG_009115.1:g.5503A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296271.4:c.361+47A>C MANE Select	ENSP00000296271.3:n.361+47A>C
ENST00000296271.3:c.361+47A>C	ENSP00000296271.3:n.361+47A>C
NM_000539.3:c.361+47A>C MANE Select	NP_000530.1:n.361+47A>C