Canonical Allele Identifier: CA546227579
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1289056583
gnomAD v2: 3-129247550-C-T
gnomAD v3: 3-129528707-C-T
gnomAD v4: 3-129528707-C-T
MyVariant Identifiers: chr3:g.129247550C>T (hg19) chr3:g.129528707C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528707C>T , CM000665.2:g.129528707C>T GRCh38
NC_000003.11:g.129247550C>T , CM000665.1:g.129247550C>T GRCh37
NC_000003.10:g.130730240C>T NCBI36
NG_009115.1:g.5069C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.-27C>T MANE Select ENSP00000296271.3:n.-27C>T
ENST00000296271.3:c.-27C>T ENSP00000296271.3:n.-27C>T
NM_000539.3:c.-27C>T MANE Select NP_000530.1:n.-27C>T
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