Canonical Allele Identifier: CA2607028
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs753353276
ExAC: 3:129247541 G / A
MyVariant Identifiers: chr3:g.129247541G>A (hg19) chr3:g.129528698G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528698G>A , CM000665.2:g.129528698G>A GRCh38
NC_000003.11:g.129247541G>A , CM000665.1:g.129247541G>A GRCh37
NC_000003.10:g.130730231G>A NCBI36
NG_009115.1:g.5060G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.-36G>A MANE Select ENSP00000296271.3:n.-36G>A
ENST00000296271.3:c.-36G>A ENSP00000296271.3:n.-36G>A
NM_000539.3:c.-36G>A MANE Select NP_000530.1:n.-36G>A
Search 100 bp 5'
Search 100 bp 3'