Canonical Allele Identifier: CA898751313

Gene: RHO

Linked Data

• dbSNP Id: rs1332092021
• gnomAD v3: 3-129530531-ACAACACACACACAC-A
• gnomAD v4: 3-129530531-ACAACACACACACAC-A
• MyVariant Identifiers: chr3:g.129249375_129249388del (hg19) ; chr3:g.129530532_129530545del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129530532_129530545del , CM000665.2:g.129530532_129530545del	GRCh38
NC_000003.11:g.129249375_129249388del , CM000665.1:g.129249375_129249388del	GRCh37
NC_000003.10:g.130732065_130732078del	NCBI36
NG_009115.1:g.6894_6907del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296271.4:c.362-344_362-331del MANE Select	ENSP00000296271.3:n.362-344_362-331del
ENST00000296271.3:c.362-344_362-331del	ENSP00000296271.3:n.362-344_362-331del
NM_000539.3:c.362-344_362-331del MANE Select	NP_000530.1:n.362-344_362-331del