Canonical Allele Identifier: CA546227575
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1354043935

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528684C>T , CM000665.2:g.129528684C>T GRCh38
NC_000003.11:g.129247527C>T , CM000665.1:g.129247527C>T GRCh37
NC_000003.10:g.130730217C>T NCBI36
NG_009115.1:g.5046C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.-50C>T MANE Select ENSP00000296271.3:n.-50C>T
ENST00000296271.3:c.-50C>T ENSP00000296271.3:n.-50C>T
NM_000539.3:c.-50C>T MANE Select NP_000530.1:n.-50C>T