Canonical Allele Identifier: CA1401211784
Gene: RHO HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532632G= , CM000665.2:g.129532632G= GRCh38
NC_000003.11:g.129251475G= , CM000665.1:g.129251475G= GRCh37
NC_000003.10:g.130734165G= NCBI36
NG_009115.1:g.8994G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.796G= MANE Select ENSP00000296271.3:p.Val266=
ENST00000296271.3:c.796G= ENSP00000296271.3:p.Val266=
NM_000539.3:c.796G= MANE Select NP_000530.1:p.Val266=
Search 100 bp 5'
Search 100 bp 3'