Canonical Allele Identifier: CA2427726113
Gene: RP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46836930A= , CM000685.2:g.46836930A= GRCh38
NC_000023.10:g.46696365A= , CM000685.1:g.46696365A= GRCh37
NC_000023.9:g.46581309A= NCBI36
NG_009107.1:g.5019A=

Transcript Alleles

HGVS Amino-acid Change
NM_006915.2:c.-171A= NP_008846.2:n.-171A=