Canonical Allele Identifier: CA2758363893
Gene: RHO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530543C>G , CM000665.2:g.129530543C>G GRCh38
NC_000003.11:g.129249386C>G , CM000665.1:g.129249386C>G GRCh37
NC_000003.10:g.130732076C>G NCBI36
NG_009115.1:g.6905C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-333C>G MANE Select ENSP00000296271.3:n.362-333C>G
ENST00000296271.3:c.362-333C>G ENSP00000296271.3:n.362-333C>G
NM_000539.3:c.362-333C>G MANE Select NP_000530.1:n.362-333C>G
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