Canonical Allele Identifier: CA354497932
Gene: RHO HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.129249736T>A (hg19) chr3:g.129530893T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129530893T>A , CM000665.2:g.129530893T>A GRCh38
NC_000003.11:g.129249736T>A , CM000665.1:g.129249736T>A GRCh37
NC_000003.10:g.130732426T>A NCBI36
NG_009115.1:g.7255T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.379T>A MANE Select ENSP00000296271.3:p.Ser127Thr
ENST00000296271.3:c.379T>A ENSP00000296271.3:p.Ser127Thr
NM_000539.3:c.379T>A MANE Select NP_000530.1:p.Ser127Thr
Search 100 bp 5'
Search 100 bp 3'