Canonical Allele Identifier: CA546228087
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1203244525
gnomAD v2: 3-129249460-C-T
gnomAD v3: 3-129530617-C-T
gnomAD v4: 3-129530617-C-T
MyVariant Identifiers: chr3:g.129249460C>T (hg19) chr3:g.129530617C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530617C>T , CM000665.2:g.129530617C>T GRCh38
NC_000003.11:g.129249460C>T , CM000665.1:g.129249460C>T GRCh37
NC_000003.10:g.130732150C>T NCBI36
NG_009115.1:g.6979C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-259C>T MANE Select ENSP00000296271.3:n.362-259C>T
ENST00000296271.3:c.362-259C>T ENSP00000296271.3:n.362-259C>T
NM_000539.3:c.362-259C>T MANE Select NP_000530.1:n.362-259C>T
Search 100 bp 5'
Search 100 bp 3'