Canonical Allele Identifier: CA2427726119
Gene: RP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46836947T= , CM000685.2:g.46836947T= GRCh38
NC_000023.10:g.46696382T= , CM000685.1:g.46696382T= GRCh37
NC_000023.9:g.46581326T= NCBI36
NG_009107.1:g.5036T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000218340.3:c.-154T= ENSP00000218340.3:n.-154T=
NM_006915.2:c.-154T= NP_008846.2:n.-154T=