Canonical Allele Identifier: CA435643828
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1213823882
gnomAD v2: 3-129249771-G-C
gnomAD v4: 3-129530928-G-C
MyVariant Identifiers: chr3:g.129249771G>C (hg19) chr3:g.129530928G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530928G>C , CM000665.2:g.129530928G>C GRCh38
NC_000003.11:g.129249771G>C , CM000665.1:g.129249771G>C GRCh37
NC_000003.10:g.130732461G>C NCBI36
NG_009115.1:g.7290G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.414G>C MANE Select ENSP00000296271.3:p.Val138=
ENST00000296271.3:c.414G>C ENSP00000296271.3:p.Val138=
NM_000539.3:c.414G>C MANE Select NP_000530.1:p.Val138=
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Search 100 bp 3'