Canonical Allele Identifier: CA898752922
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1443314566

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532169C>T , CM000665.2:g.129532169C>T GRCh38
NC_000003.11:g.129251012C>T , CM000665.1:g.129251012C>T GRCh37
NC_000003.10:g.130733702C>T NCBI36
NG_009115.1:g.8531C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.531-82C>T MANE Select ENSP00000296271.3:n.531-82C>T
ENST00000296271.3:c.531-82C>T ENSP00000296271.3:n.531-82C>T
NM_000539.3:c.531-82C>T MANE Select NP_000530.1:n.531-82C>T