Canonical Allele Identifier: CA354470572
Gene: RHO HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.129251527T>A (hg19) chr3:g.129532684T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532684T>A , CM000665.2:g.129532684T>A GRCh38
NC_000003.11:g.129251527T>A , CM000665.1:g.129251527T>A GRCh37
NC_000003.10:g.130734217T>A NCBI36
NG_009115.1:g.9046T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.848T>A MANE Select ENSP00000296271.3:p.Phe283Tyr
ENST00000296271.3:c.848T>A ENSP00000296271.3:p.Phe283Tyr
NM_000539.3:c.848T>A MANE Select NP_000530.1:p.Phe283Tyr
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