Canonical Allele Identifier: CA2693550276
Gene: RP2 HGNC NCBI

Linked Data

gnomAD v4: X-46836939-AGG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46836942_46836943del , CM000685.2:g.46836942_46836943del GRCh38
NC_000023.10:g.46696377_46696378del , CM000685.1:g.46696377_46696378del GRCh37
NC_000023.9:g.46581321_46581322del NCBI36
NG_009107.1:g.5031_5032del

Transcript Alleles

HGVS Amino-acid Change
ENST00000218340.3:c.-159_-158del ENSP00000218340.3:n.-159_-158del
NM_006915.2:c.-159_-158del NP_008846.2:n.-159_-158del
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