Canonical Allele Identifier: CA354471161
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs749663446
gnomAD v4: 3-129533650-C-A
MyVariant Identifiers: chr3:g.129252493C>A (hg19) chr3:g.129533650C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129533650C>A , CM000665.2:g.129533650C>A GRCh38
NC_000003.11:g.129252493C>A , CM000665.1:g.129252493C>A GRCh37
NC_000003.10:g.130735183C>A NCBI36
NG_009115.1:g.10012C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.979C>A MANE Select ENSP00000296271.3:p.Pro327Thr
ENST00000296271.3:c.979C>A ENSP00000296271.3:p.Pro327Thr
NM_000539.3:c.979C>A MANE Select NP_000530.1:p.Pro327Thr
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