Canonical Allele Identifier: CA2693550266
Gene: RP2 HGNC NCBI

Linked Data

gnomAD v4: X-46836924-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46836924C>T , CM000685.2:g.46836924C>T GRCh38
NC_000023.10:g.46696359C>T , CM000685.1:g.46696359C>T GRCh37
NC_000023.9:g.46581303C>T NCBI36
NG_009107.1:g.5013C>T

Transcript Alleles

HGVS Amino-acid Change
NM_006915.2:c.-177C>T NP_008846.2:n.-177C>T