Canonical Allele Identifier: CA435644077
Gene: RHO HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.129249837C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530994C>G , CM000665.2:g.129530994C>G GRCh38
NC_000003.11:g.129249837C>G , CM000665.1:g.129249837C>G GRCh37
NC_000003.10:g.130732527C>G NCBI36
NG_009115.1:g.7356C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.480C>G MANE Select ENSP00000296271.3:p.Thr160=
ENST00000296271.3:c.480C>G ENSP00000296271.3:p.Thr160=
NM_000539.3:c.480C>G MANE Select NP_000530.1:p.Thr160=