Canonical Allele Identifier: CA1401206827
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084761322
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529402G>T , CM000665.2:g.129529402G>T GRCh38
NC_000003.11:g.129248245G>T , CM000665.1:g.129248245G>T GRCh37
NC_000003.10:g.130730935G>T NCBI36
NG_009115.1:g.5764G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+308G>T MANE Select ENSP00000296271.3:n.361+308G>T
ENST00000296271.3:c.361+308G>T ENSP00000296271.3:n.361+308G>T
NM_000539.3:c.361+308G>T MANE Select NP_000530.1:n.361+308G>T
Search 100 bp 5'
Search 100 bp 3'