Canonical Allele Identifier: CA2667616696
Gene: RHO HGNC NCBI

Linked Data

gnomAD v4: 3-129532226-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532226G>C , CM000665.2:g.129532226G>C GRCh38
NC_000003.11:g.129251069G>C , CM000665.1:g.129251069G>C GRCh37
NC_000003.10:g.130733759G>C NCBI36
NG_009115.1:g.8588G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.531-25G>C MANE Select ENSP00000296271.3:n.531-25G>C
ENST00000296271.3:c.531-25G>C ENSP00000296271.3:n.531-25G>C
NM_000539.3:c.531-25G>C MANE Select NP_000530.1:n.531-25G>C
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