Canonical Allele Identifier: CA2427726105
Gene: RP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46836915T= , CM000685.2:g.46836915T= GRCh38
NC_000023.10:g.46696350T= , CM000685.1:g.46696350T= GRCh37
NC_000023.9:g.46581294T= NCBI36
NG_009107.1:g.5004T=

Transcript Alleles

HGVS Amino-acid Change
NM_006915.2:c.-186T= NP_008846.2:n.-186T=