Canonical Allele Identifier: CA2758363809
Gene: RHO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129529238_129529239insA , CM000665.2:g.129529238_129529239insA GRCh38
NC_000003.11:g.129248081_129248082insA , CM000665.1:g.129248081_129248082insA GRCh37
NC_000003.10:g.130730771_130730772insA NCBI36
NG_009115.1:g.5600_5601insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296271.4:c.361+144_361+145insA MANE Select ENSP00000296271.3:n.361+144_361+145insA
ENST00000296271.3:c.361+144_361+145insA ENSP00000296271.3:n.361+144_361+145insA
NM_000539.3:c.361+144_361+145insA MANE Select NP_000530.1:n.361+144_361+145insA