Canonical Allele Identifier: CA2693550297
Gene: RP2 HGNC NCBI

Linked Data

gnomAD v4: X-46836957-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46836957G>T , CM000685.2:g.46836957G>T GRCh38
NC_000023.10:g.46696392G>T , CM000685.1:g.46696392G>T GRCh37
NC_000023.9:g.46581336G>T NCBI36
NG_009107.1:g.5046G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000218340.3:c.-144G>T ENSP00000218340.3:n.-144G>T
NM_006915.2:c.-144G>T NP_008846.2:n.-144G>T
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