Canonical Allele Identifier: CA898752353
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1232361259
MyVariant Identifiers: chr3:g.129249982T>C (hg19) chr3:g.129531139T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129531139T>C , CM000665.2:g.129531139T>C GRCh38
NC_000003.11:g.129249982T>C , CM000665.1:g.129249982T>C GRCh37
NC_000003.10:g.130732672T>C NCBI36
NG_009115.1:g.7501T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.530+95T>C MANE Select ENSP00000296271.3:n.530+95T>C
ENST00000296271.3:c.530+95T>C ENSP00000296271.3:n.530+95T>C
NM_000539.3:c.530+95T>C MANE Select NP_000530.1:n.530+95T>C
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