Canonical Allele Identifier: CA354499053
Gene: RHO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129532251G>T , CM000665.2:g.129532251G>T GRCh38
NC_000003.11:g.129251094G>T , CM000665.1:g.129251094G>T GRCh37
NC_000003.10:g.130733784G>T NCBI36
NG_009115.1:g.8613G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000296271.4:c.531G>T MANE Select ENSP00000296271.3:p.Arg177Ser
ENST00000296271.3:c.531G>T ENSP00000296271.3:p.Arg177Ser
NM_000539.3:c.531G>T MANE Select NP_000530.1:p.Arg177Ser