Canonical Allele Identifier: CA898751653
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1253057494
MyVariant Identifiers: chr3:g.129249529_129249530insCTCC (hg19) chr3:g.129530686_129530687insCTCC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530687_129530690dup , CM000665.2:g.129530687_129530690dup GRCh38
NC_000003.11:g.129249530_129249533dup , CM000665.1:g.129249530_129249533dup GRCh37
NC_000003.10:g.130732220_130732223dup NCBI36
NG_009115.1:g.7049_7052dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-189_362-186dup MANE Select ENSP00000296271.3:n.362-189_362-186dup
ENST00000296271.3:c.362-189_362-186dup ENSP00000296271.3:n.362-189_362-186dup
NM_000539.3:c.362-189_362-186dup MANE Select NP_000530.1:n.362-189_362-186dup
Search 100 bp 5'
Search 100 bp 3'