Canonical Allele Identifier: CA2820729967
Gene: RP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46836929A>C , CM000685.2:g.46836929A>C GRCh38
NC_000023.10:g.46696364A>C , CM000685.1:g.46696364A>C GRCh37
NC_000023.9:g.46581308A>C NCBI36
NG_009107.1:g.5018A>C

Transcript Alleles

HGVS Amino-acid Change
NM_006915.2:c.-172A>C NP_008846.2:n.-172A>C
Search 100 bp 5'
Search 100 bp 3'