Canonical Allele Identifier: CA354496961
Gene: RHO HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.129247916G>A (hg19) chr3:g.129529073G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529073G>A , CM000665.2:g.129529073G>A GRCh38
NC_000003.11:g.129247916G>A , CM000665.1:g.129247916G>A GRCh37
NC_000003.10:g.130730606G>A NCBI36
NG_009115.1:g.5435G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.340G>A MANE Select ENSP00000296271.3:p.Gly114Ser
ENST00000296271.3:c.340G>A ENSP00000296271.3:p.Gly114Ser
NM_000539.3:c.340G>A MANE Select NP_000530.1:p.Gly114Ser
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Search 100 bp 3'