Canonical Allele Identifier: CA1132850926
Gene: RP2 HGNC NCBI

Linked Data

dbSNP Id: rs1924509310
gnomAD v3: X-46836930-A-G
gnomAD v4: X-46836930-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46836930A>G , CM000685.2:g.46836930A>G GRCh38
NC_000023.10:g.46696365A>G , CM000685.1:g.46696365A>G GRCh37
NC_000023.9:g.46581309A>G NCBI36
NG_009107.1:g.5019A>G

Transcript Alleles

HGVS Amino-acid Change
NM_006915.2:c.-171A>G NP_008846.2:n.-171A>G