Canonical Allele Identifier: CA435644698
Gene: RHO HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.129251124T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532281T>C , CM000665.2:g.129532281T>C GRCh38
NC_000003.11:g.129251124T>C , CM000665.1:g.129251124T>C GRCh37
NC_000003.10:g.130733814T>C NCBI36
NG_009115.1:g.8643T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.561T>C MANE Select ENSP00000296271.3:p.Cys187=
ENST00000296271.3:c.561T>C ENSP00000296271.3:p.Cys187=
NM_000539.3:c.561T>C MANE Select NP_000530.1:p.Cys187=
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