Canonical Allele Identifier: CA354496958
Gene: RHO HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.129247916G>T (hg19) chr3:g.129529073G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529073G>T , CM000665.2:g.129529073G>T GRCh38
NC_000003.11:g.129247916G>T , CM000665.1:g.129247916G>T GRCh37
NC_000003.10:g.130730606G>T NCBI36
NG_009115.1:g.5435G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.340G>T MANE Select ENSP00000296271.3:p.Gly114Cys
ENST00000296271.3:c.340G>T ENSP00000296271.3:p.Gly114Cys
NM_000539.3:c.340G>T MANE Select NP_000530.1:p.Gly114Cys
Search 100 bp 5'
Search 100 bp 3'