Canonical Allele Identifier: CA435768861
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs753585848
MyVariant Identifiers: chr3:g.129247627G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528784G>T , CM000665.2:g.129528784G>T GRCh38
NC_000003.11:g.129247627G>T , CM000665.1:g.129247627G>T GRCh37
NC_000003.10:g.130730317G>T NCBI36
NG_009115.1:g.5146G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.51G>T MANE Select ENSP00000296271.3:p.Thr17=
ENST00000296271.3:c.51G>T ENSP00000296271.3:p.Thr17=
NM_000539.3:c.51G>T MANE Select NP_000530.1:p.Thr17=