Canonical Allele Identifier: CA1401208979
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1578279426
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530618G>A , CM000665.2:g.129530618G>A GRCh38
NC_000003.11:g.129249461G>A , CM000665.1:g.129249461G>A GRCh37
NC_000003.10:g.130732151G>A NCBI36
NG_009115.1:g.6980G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-258G>A MANE Select ENSP00000296271.3:n.362-258G>A
ENST00000296271.3:c.362-258G>A ENSP00000296271.3:n.362-258G>A
NM_000539.3:c.362-258G>A MANE Select NP_000530.1:n.362-258G>A
Search 100 bp 5'
Search 100 bp 3'