Canonical Allele Identifier: CA329690598
Gene: RP2 HGNC NCBI

Linked Data

dbSNP Id: rs957096405
gnomAD v2: X-46696368-A-G
gnomAD v3: X-46836933-A-G
gnomAD v4: X-46836933-A-G
MyVariant Identifiers: chrX:g.46696368A>G (hg19) chrX:g.46836933A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46836933A>G , CM000685.2:g.46836933A>G GRCh38
NC_000023.10:g.46696368A>G , CM000685.1:g.46696368A>G GRCh37
NC_000023.9:g.46581312A>G NCBI36
NG_009107.1:g.5022A>G

Transcript Alleles

HGVS Amino-acid Change
NM_006915.2:c.-168A>G NP_008846.2:n.-168A>G
Search 100 bp 5'
Search 100 bp 3'