Canonical Allele Identifier: CA2667614630
Gene: RHO HGNC NCBI

Linked Data

gnomAD v4: 3-129528690-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528690T>G , CM000665.2:g.129528690T>G GRCh38
NC_000003.11:g.129247533T>G , CM000665.1:g.129247533T>G GRCh37
NC_000003.10:g.130730223T>G NCBI36
NG_009115.1:g.5052T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.-44T>G MANE Select ENSP00000296271.3:n.-44T>G
ENST00000296271.3:c.-44T>G ENSP00000296271.3:n.-44T>G
NM_000539.3:c.-44T>G MANE Select NP_000530.1:n.-44T>G
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