Canonical Allele Identifier: CA1401212994
Gene: RHO HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129533568T= , CM000665.2:g.129533568T= GRCh38
NC_000003.11:g.129252411T= , CM000665.1:g.129252411T= GRCh37
NC_000003.10:g.130735101T= NCBI36
NG_009115.1:g.9930T=

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.937-40T= MANE Select ENSP00000296271.3:n.937-40T=
ENST00000296271.3:c.937-40T= ENSP00000296271.3:n.937-40T=
NM_000539.3:c.937-40T= MANE Select NP_000530.1:n.937-40T=
Search 100 bp 5'
Search 100 bp 3'