Canonical Allele Identifier: CA1401208147
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs2084770558
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530515_129530525dup , CM000665.2:g.129530515_129530525dup GRCh38
NC_000003.11:g.129249358_129249368dup , CM000665.1:g.129249358_129249368dup GRCh37
NC_000003.10:g.130732048_130732058dup NCBI36
NG_009115.1:g.6877_6887dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-361_362-351dup MANE Select ENSP00000296271.3:n.362-361_362-351dup
ENST00000296271.3:c.362-361_362-351dup ENSP00000296271.3:n.362-361_362-351dup
NM_000539.3:c.362-361_362-351dup MANE Select NP_000530.1:n.362-361_362-351dup
Search 100 bp 5'
Search 100 bp 3'