Canonical Allele Identifier: CA2667617058
Gene: RHO HGNC NCBI

Linked Data

gnomAD v4: 3-129532431-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532431G>C , CM000665.2:g.129532431G>C GRCh38
NC_000003.11:g.129251274G>C , CM000665.1:g.129251274G>C GRCh37
NC_000003.10:g.130733964G>C NCBI36
NG_009115.1:g.8793G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.696+15G>C MANE Select ENSP00000296271.3:n.696+15G>C
ENST00000296271.3:c.696+15G>C ENSP00000296271.3:n.696+15G>C
NM_000539.3:c.696+15G>C MANE Select NP_000530.1:n.696+15G>C
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