Canonical Allele Identifier: CA354470815
Gene: RHO HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.129251569G>T (hg19) chr3:g.129532726G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532726G>T , CM000665.2:g.129532726G>T GRCh38
NC_000003.11:g.129251569G>T , CM000665.1:g.129251569G>T GRCh37
NC_000003.10:g.130734259G>T NCBI36
NG_009115.1:g.9088G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.890G>T MANE Select ENSP00000296271.3:p.Ser297Ile
ENST00000296271.3:c.890G>T ENSP00000296271.3:p.Ser297Ile
NM_000539.3:c.890G>T MANE Select NP_000530.1:p.Ser297Ile
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