Canonical Allele Identifier: CA2667618270
Gene: RHO HGNC NCBI

Linked Data

gnomAD v4: 3-129533564-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129533564A>G , CM000665.2:g.129533564A>G GRCh38
NC_000003.11:g.129252407A>G , CM000665.1:g.129252407A>G GRCh37
NC_000003.10:g.130735097A>G NCBI36
NG_009115.1:g.9926A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.937-44A>G MANE Select ENSP00000296271.3:n.937-44A>G
ENST00000296271.3:c.937-44A>G ENSP00000296271.3:n.937-44A>G
NM_000539.3:c.937-44A>G MANE Select NP_000530.1:n.937-44A>G
Search 100 bp 5'
Search 100 bp 3'