Canonical Allele Identifier: CA2758363607
Gene: RHO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528695G>T , CM000665.2:g.129528695G>T GRCh38
NC_000003.11:g.129247538G>T , CM000665.1:g.129247538G>T GRCh37
NC_000003.10:g.130730228G>T NCBI36
NG_009115.1:g.5057G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.-39G>T MANE Select ENSP00000296271.3:n.-39G>T
ENST00000296271.3:c.-39G>T ENSP00000296271.3:n.-39G>T
NM_000539.3:c.-39G>T MANE Select NP_000530.1:n.-39G>T
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