Canonical Allele Identifier: CA1401212054
Gene: RHO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532743C= , CM000665.2:g.129532743C= GRCh38
NC_000003.11:g.129251586C= , CM000665.1:g.129251586C= GRCh37
NC_000003.10:g.130734276C= NCBI36
NG_009115.1:g.9105C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.907C= MANE Select ENSP00000296271.3:p.Pro303=
ENST00000296271.3:c.907C= ENSP00000296271.3:p.Pro303=
NM_000539.3:c.907C= MANE Select NP_000530.1:p.Pro303=
Search 100 bp 5'
Search 100 bp 3'