Canonical Allele Identifier: CA2693550271
Gene: RP2 HGNC NCBI

Linked Data

gnomAD v4: X-46836928-GA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46836933del , CM000685.2:g.46836933del GRCh38
NC_000023.10:g.46696368del , CM000685.1:g.46696368del GRCh37
NC_000023.9:g.46581312del NCBI36
NG_009107.1:g.5022del

Transcript Alleles

HGVS Amino-acid Change
NM_006915.2:c.-168del NP_008846.2:n.-168del
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