Canonical Allele Identifier: CA2693550258
Gene: RP2 HGNC NCBI

Linked Data

gnomAD v4: X-46836911-T-TG
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46836914dup , CM000685.2:g.46836914dup GRCh38
NC_000023.10:g.46696349dup , CM000685.1:g.46696349dup GRCh37
NC_000023.9:g.46581293dup NCBI36
NG_009107.1:g.5003dup

Transcript Alleles

HGVS Amino-acid Change
NM_006915.2:c.-187dup NP_008846.2:n.-187dup
Search 100 bp 5'
Search 100 bp 3'