Canonical Allele Identifier: CA898750769
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1245384573
MyVariant Identifiers: chr3:g.129248168T>A (hg19) chr3:g.129529325T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529325T>A , CM000665.2:g.129529325T>A GRCh38
NC_000003.11:g.129248168T>A , CM000665.1:g.129248168T>A GRCh37
NC_000003.10:g.130730858T>A NCBI36
NG_009115.1:g.5687T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+231T>A MANE Select ENSP00000296271.3:n.361+231T>A
ENST00000296271.3:c.361+231T>A ENSP00000296271.3:n.361+231T>A
NM_000539.3:c.361+231T>A MANE Select NP_000530.1:n.361+231T>A
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