Canonical Allele Identifier: CA2607087
Gene: RHO HGNC NCBI

Linked Data

ClinVar Variation Id: 834861
ClinVar RCV Id: RCV001035632 RCV003483756
dbSNP Id: rs143559914
ExAC: 3:129247785 C / T
gnomAD v2: 3-129247785-C-T
gnomAD v3: 3-129528942-C-T
gnomAD v4: 3-129528942-C-T
COSMIC: COSM1418834
MyVariant Identifiers: chr3:g.129247785C>T (hg19) chr3:g.129528942C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528942C>T , CM000665.2:g.129528942C>T GRCh38
NC_000003.11:g.129247785C>T , CM000665.1:g.129247785C>T GRCh37
NC_000003.10:g.130730475C>T NCBI36
NG_009115.1:g.5304C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.209C>T MANE Select ENSP00000296271.3:p.Thr70Met
ENST00000296271.3:c.209C>T ENSP00000296271.3:p.Thr70Met
NM_000539.3:c.209C>T MANE Select NP_000530.1:p.Thr70Met
Search 100 bp 5'
Search 100 bp 3'