Canonical Allele Identifier: CA435768922
Gene: RHO HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.129247723G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528880G>A , CM000665.2:g.129528880G>A GRCh38
NC_000003.11:g.129247723G>A , CM000665.1:g.129247723G>A GRCh37
NC_000003.10:g.130730413G>A NCBI36
NG_009115.1:g.5242G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.147G>A MANE Select ENSP00000296271.3:p.Val49=
ENST00000296271.3:c.147G>A ENSP00000296271.3:p.Val49=
NM_000539.3:c.147G>A MANE Select NP_000530.1:p.Val49=
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