Canonical Allele Identifier: CA2667616059
Gene: RHO HGNC NCBI

Linked Data

gnomAD v4: 3-129530798-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530798C>A , CM000665.2:g.129530798C>A GRCh38
NC_000003.11:g.129249641C>A , CM000665.1:g.129249641C>A GRCh37
NC_000003.10:g.130732331C>A NCBI36
NG_009115.1:g.7160C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.362-78C>A MANE Select ENSP00000296271.3:n.362-78C>A
ENST00000296271.3:c.362-78C>A ENSP00000296271.3:n.362-78C>A
NM_000539.3:c.362-78C>A MANE Select NP_000530.1:n.362-78C>A
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