Canonical Allele Identifier: CA898751556
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1169200718
gnomAD v3: 3-129530552-A-G
gnomAD v4: 3-129530552-A-G
MyVariant Identifiers: chr3:g.129249395A>G (hg19) chr3:g.129530552A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530552A>G , CM000665.2:g.129530552A>G GRCh38
NC_000003.11:g.129249395A>G , CM000665.1:g.129249395A>G GRCh37
NC_000003.10:g.130732085A>G NCBI36
NG_009115.1:g.6914A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.362-324A>G MANE Select ENSP00000296271.3:n.362-324A>G
ENST00000296271.3:c.362-324A>G ENSP00000296271.3:n.362-324A>G
NM_000539.3:c.362-324A>G MANE Select NP_000530.1:n.362-324A>G
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Search 100 bp 3'