Canonical Allele Identifier: CA435644125
Gene: RHO HGNC NCBI

Linked Data

gnomAD v4: 3-129531006-G-T
MyVariant Identifiers: chr3:g.129249849G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129531006G>T , CM000665.2:g.129531006G>T GRCh38
NC_000003.11:g.129249849G>T , CM000665.1:g.129249849G>T GRCh37
NC_000003.10:g.130732539G>T NCBI36
NG_009115.1:g.7368G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.492G>T MANE Select ENSP00000296271.3:p.Ala164=
ENST00000296271.3:c.492G>T ENSP00000296271.3:p.Ala164=
NM_000539.3:c.492G>T MANE Select NP_000530.1:p.Ala164=
Search 100 bp 5'
Search 100 bp 3'