Canonical Allele Identifier: CA2607328
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs747582133
ExAC: 3:129252406 C / T
gnomAD v2: 3-129252406-C-T
gnomAD v4: 3-129533563-C-T
MyVariant Identifiers: chr3:g.129252406C>T (hg19) chr3:g.129533563C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129533563C>T , CM000665.2:g.129533563C>T GRCh38
NC_000003.11:g.129252406C>T , CM000665.1:g.129252406C>T GRCh37
NC_000003.10:g.130735096C>T NCBI36
NG_009115.1:g.9925C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.937-45C>T MANE Select ENSP00000296271.3:n.937-45C>T
ENST00000296271.3:c.937-45C>T ENSP00000296271.3:n.937-45C>T
NM_000539.3:c.937-45C>T MANE Select NP_000530.1:n.937-45C>T
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