Canonical Allele Identifier: CA2579593008
Gene: RP2 HGNC NCBI

Linked Data

gnomAD v4: X-46837012-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46837012C>A , CM000685.2:g.46837012C>A GRCh38
NC_000023.10:g.46696447C>A , CM000685.1:g.46696447C>A GRCh37
NC_000023.9:g.46581391C>A NCBI36
NG_009107.1:g.5101C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000218340.3:c.-89C>A ENSP00000218340.3:n.-89C>A
NM_006915.2:c.-89C>A NP_008846.2:n.-89C>A
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