Canonical Allele Identifier: CA82648122
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs766932095
gnomAD v2: 3-129249375-CA-C
gnomAD v3: 3-129530532-CA-C
gnomAD v4: 3-129530532-CA-C
MyVariant Identifiers: chr3:g.129249376del (hg19) chr3:g.129249377_129249379delinsCA (hg19) chr3:g.129530533del (hg38) chr3:g.129530534_129530536delinsCA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530534del , CM000665.2:g.129530534del GRCh38
NC_000003.11:g.129249377del , CM000665.1:g.129249377del GRCh37
NC_000003.10:g.130732067del NCBI36
NG_009115.1:g.6896del

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-342del MANE Select ENSP00000296271.3:n.362-342del
ENST00000296271.3:c.362-342del ENSP00000296271.3:n.362-342del
NM_000539.3:c.362-342del MANE Select NP_000530.1:n.362-342del
Search 100 bp 5'
Search 100 bp 3'