Canonical Allele Identifier: CA2427726130
Gene: RP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46836960C= , CM000685.2:g.46836960C= GRCh38
NC_000023.10:g.46696395C= , CM000685.1:g.46696395C= GRCh37
NC_000023.9:g.46581339C= NCBI36
NG_009107.1:g.5049C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000218340.3:c.-141C= ENSP00000218340.3:n.-141C=
NM_006915.2:c.-141C= NP_008846.2:n.-141C=