Canonical Allele Identifier: CA2427726115
Gene: RP2 HGNC NCBI

Linked Data

dbSNP Id: rs1924509459

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46836932A>C , CM000685.2:g.46836932A>C GRCh38
NC_000023.10:g.46696367A>C , CM000685.1:g.46696367A>C GRCh37
NC_000023.9:g.46581311A>C NCBI36
NG_009107.1:g.5021A>C

Transcript Alleles

HGVS Amino-acid Change
NM_006915.2:c.-169A>C NP_008846.2:n.-169A>C