Canonical Allele Identifier: CA354496368
Gene: RHO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129528954A>T , CM000665.2:g.129528954A>T GRCh38
NC_000003.11:g.129247797A>T , CM000665.1:g.129247797A>T GRCh37
NC_000003.10:g.130730487A>T NCBI36
NG_009115.1:g.5316A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.221A>T MANE Select ENSP00000296271.3:p.Tyr74Phe
ENST00000296271.3:c.221A>T ENSP00000296271.3:p.Tyr74Phe
NM_000539.3:c.221A>T MANE Select NP_000530.1:p.Tyr74Phe