Canonical Allele Identifier: CA354470766
Gene: RHO HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.129251561T>G (hg19) chr3:g.129532718T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532718T>G , CM000665.2:g.129532718T>G GRCh38
NC_000003.11:g.129251561T>G , CM000665.1:g.129251561T>G GRCh37
NC_000003.10:g.130734251T>G NCBI36
NG_009115.1:g.9080T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.882T>G MANE Select ENSP00000296271.3:p.Phe294Leu
ENST00000296271.3:c.882T>G ENSP00000296271.3:p.Phe294Leu
NM_000539.3:c.882T>G MANE Select NP_000530.1:p.Phe294Leu
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