Canonical Allele Identifier: CA435768707
Gene: RHO HGNC NCBI

Linked Data

COSMIC: COSM6163251
MyVariant Identifiers: chr3:g.129247828C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528985C>G , CM000665.2:g.129528985C>G GRCh38
NC_000003.11:g.129247828C>G , CM000665.1:g.129247828C>G GRCh37
NC_000003.10:g.130730518C>G NCBI36
NG_009115.1:g.5347C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.252C>G MANE Select ENSP00000296271.3:p.Leu84=
ENST00000296271.3:c.252C>G ENSP00000296271.3:p.Leu84=
NM_000539.3:c.252C>G MANE Select NP_000530.1:p.Leu84=
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