Canonical Allele Identifier: CA82647132
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs372128112

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529104G>T , CM000665.2:g.129529104G>T GRCh38
NC_000003.11:g.129247947G>T , CM000665.1:g.129247947G>T GRCh37
NC_000003.10:g.130730637G>T NCBI36
NG_009115.1:g.5466G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+10G>T MANE Select ENSP00000296271.3:n.361+10G>T
ENST00000296271.3:c.361+10G>T ENSP00000296271.3:n.361+10G>T
NM_000539.3:c.361+10G>T MANE Select NP_000530.1:n.361+10G>T