Canonical Allele Identifier: CA2427726142
Gene: RP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46836978C= , CM000685.2:g.46836978C= GRCh38
NC_000023.10:g.46696413C= , CM000685.1:g.46696413C= GRCh37
NC_000023.9:g.46581357C= NCBI36
NG_009107.1:g.5067C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000218340.3:c.-123C= ENSP00000218340.3:n.-123C=
NM_006915.2:c.-123C= NP_008846.2:n.-123C=