Canonical Allele Identifier: CA1401211321
Gene: RHO HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532421G= , CM000665.2:g.129532421G= GRCh38
NC_000003.11:g.129251264G= , CM000665.1:g.129251264G= GRCh37
NC_000003.10:g.130733954G= NCBI36
NG_009115.1:g.8783G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.696+5G= MANE Select ENSP00000296271.3:n.696+5G=
ENST00000296271.3:c.696+5G= ENSP00000296271.3:n.696+5G=
NM_000539.3:c.696+5G= MANE Select NP_000530.1:n.696+5G=
Search 100 bp 5'
Search 100 bp 3'