Canonical Allele Identifier: CA546417832

Gene: RHO

Linked Data

• dbSNP Id: rs1472077837
• gnomAD v2: 3-129251327-C-T
• gnomAD v4: 3-129532484-C-T
• MyVariant Identifiers: chr3:g.129251327C>T (hg19) ; chr3:g.129532484C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129532484C>T , CM000665.2:g.129532484C>T	GRCh38
NC_000003.11:g.129251327C>T , CM000665.1:g.129251327C>T	GRCh37
NC_000003.10:g.130734017C>T	NCBI36
NG_009115.1:g.8846C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000296271.4:c.697-49C>T MANE Select	ENSP00000296271.3:n.697-49C>T
ENST00000296271.3:c.697-49C>T	ENSP00000296271.3:n.697-49C>T
NM_000539.3:c.697-49C>T MANE Select	NP_000530.1:n.697-49C>T