Canonical Allele Identifier: CA2427726129
Gene: RP2 HGNC NCBI

Linked Data

dbSNP Id: rs1924510684

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46836960del , CM000685.2:g.46836960del GRCh38
NC_000023.10:g.46696395del , CM000685.1:g.46696395del GRCh37
NC_000023.9:g.46581339del NCBI36
NG_009107.1:g.5049del

Transcript Alleles

HGVS Amino-acid Change
ENST00000218340.3:c.-141del ENSP00000218340.3:n.-141del
NM_006915.2:c.-141del NP_008846.2:n.-141del