Canonical Allele Identifier: CA82649491
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1048978598
MyVariant Identifiers: chr3:g.129250688A>C (hg19) chr3:g.129531845A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129531845A>C , CM000665.2:g.129531845A>C GRCh38
NC_000003.11:g.129250688A>C , CM000665.1:g.129250688A>C GRCh37
NC_000003.10:g.130733378A>C NCBI36
NG_009115.1:g.8207A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.531-406A>C MANE Select ENSP00000296271.3:n.531-406A>C
ENST00000296271.3:c.531-406A>C ENSP00000296271.3:n.531-406A>C
NM_000539.3:c.531-406A>C MANE Select NP_000530.1:n.531-406A>C
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