Canonical Allele Identifier: CA2693550265
Gene: RP2 HGNC NCBI

Linked Data

gnomAD v4: X-46836918-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46836918T>C , CM000685.2:g.46836918T>C GRCh38
NC_000023.10:g.46696353T>C , CM000685.1:g.46696353T>C GRCh37
NC_000023.9:g.46581297T>C NCBI36
NG_009107.1:g.5007T>C

Transcript Alleles

HGVS Amino-acid Change
NM_006915.2:c.-183T>C NP_008846.2:n.-183T>C
Search 100 bp 5'
Search 100 bp 3'