Canonical Allele Identifier: CA354495931
Gene: RHO HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.129247722T>G (hg19) chr3:g.129528879T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528879T>G , CM000665.2:g.129528879T>G GRCh38
NC_000003.11:g.129247722T>G , CM000665.1:g.129247722T>G GRCh37
NC_000003.10:g.130730412T>G NCBI36
NG_009115.1:g.5241T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.146T>G MANE Select ENSP00000296271.3:p.Val49Gly
ENST00000296271.3:c.146T>G ENSP00000296271.3:p.Val49Gly
NM_000539.3:c.146T>G MANE Select NP_000530.1:p.Val49Gly
Search 100 bp 5'
Search 100 bp 3'