Canonical Allele Identifier: CA354496082
Gene: RHO HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.129247755A>G (hg19) chr3:g.129528912A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528912A>G , CM000665.2:g.129528912A>G GRCh38
NC_000003.11:g.129247755A>G , CM000665.1:g.129247755A>G GRCh37
NC_000003.10:g.130730445A>G NCBI36
NG_009115.1:g.5274A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.179A>G MANE Select ENSP00000296271.3:p.Tyr60Cys
ENST00000296271.3:c.179A>G ENSP00000296271.3:p.Tyr60Cys
NM_000539.3:c.179A>G MANE Select NP_000530.1:p.Tyr60Cys
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