Canonical Allele Identifier: CA2427726108
Gene: RP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46836922G= , CM000685.2:g.46836922G= GRCh38
NC_000023.10:g.46696357G= , CM000685.1:g.46696357G= GRCh37
NC_000023.9:g.46581301G= NCBI36
NG_009107.1:g.5011G=

Transcript Alleles

HGVS Amino-acid Change
NM_006915.2:c.-179G= NP_008846.2:n.-179G=