Canonical Allele Identifier: CA898749617
Gene: RHO HGNC NCBI

Linked Data

dbSNP Id: rs1245135960
MyVariant Identifiers: chr3:g.129247528A>T (hg19) chr3:g.129528685A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528685A>T , CM000665.2:g.129528685A>T GRCh38
NC_000003.11:g.129247528A>T , CM000665.1:g.129247528A>T GRCh37
NC_000003.10:g.130730218A>T NCBI36
NG_009115.1:g.5047A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.-49A>T MANE Select ENSP00000296271.3:n.-49A>T
ENST00000296271.3:c.-49A>T ENSP00000296271.3:n.-49A>T
NM_000539.3:c.-49A>T MANE Select NP_000530.1:n.-49A>T
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