Canonical Allele Identifier: CA2607049
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs757740913
ExAC: 3:129247633 G / A
gnomAD v2: 3-129247633-G-A
gnomAD v4: 3-129528790-G-A
MyVariant Identifiers: chr3:g.129247633G>A (hg19) chr3:g.129528790G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528790G>A , CM000665.2:g.129528790G>A GRCh38
NC_000003.11:g.129247633G>A , CM000665.1:g.129247633G>A GRCh37
NC_000003.10:g.130730323G>A NCBI36
NG_009115.1:g.5152G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.57G>A MANE Select ENSP00000296271.3:p.Val19=
ENST00000296271.3:c.57G>A ENSP00000296271.3:p.Val19=
NM_000539.3:c.57G>A MANE Select NP_000530.1:p.Val19=
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Search 100 bp 3'