Canonical Allele Identifier: CA2820729969
Gene: RP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46836988T>G , CM000685.2:g.46836988T>G GRCh38
NC_000023.10:g.46696423T>G , CM000685.1:g.46696423T>G GRCh37
NC_000023.9:g.46581367T>G NCBI36
NG_009107.1:g.5077T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000218340.3:c.-113T>G ENSP00000218340.3:n.-113T>G
NM_006915.2:c.-113T>G NP_008846.2:n.-113T>G