Canonical Allele Identifier: CA435643939
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 1088237
ClinVar RCV Id: RCV001406645
dbSNP Id: rs1297879534
gnomAD v2: 3-129249804-G-A
gnomAD v3: 3-129530961-G-A
gnomAD v4: 3-129530961-G-A
COSMIC: COSM4548442
MyVariant Identifiers: chr3:g.129249804G>A (hg19) chr3:g.129530961G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530961G>A , CM000665.2:g.129530961G>A GRCh38
NC_000003.11:g.129249804G>A , CM000665.1:g.129249804G>A GRCh37
NC_000003.10:g.130732494G>A NCBI36
NG_009115.1:g.7323G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.447G>A MANE Select ENSP00000296271.3:p.Gly149=
ENST00000296271.3:c.447G>A ENSP00000296271.3:p.Gly149=
NM_000539.3:c.447G>A MANE Select NP_000530.1:p.Gly149=
Search 100 bp 5'
Search 100 bp 3'