Canonical Allele Identifier: CA1401212999
Gene: RHO HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129533570G= , CM000665.2:g.129533570G= GRCh38
NC_000003.11:g.129252413G= , CM000665.1:g.129252413G= GRCh37
NC_000003.10:g.130735103G= NCBI36
NG_009115.1:g.9932G=

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.937-38G= MANE Select ENSP00000296271.3:n.937-38G=
ENST00000296271.3:c.937-38G= ENSP00000296271.3:n.937-38G=
NM_000539.3:c.937-38G= MANE Select NP_000530.1:n.937-38G=
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