Canonical Allele Identifier: CA875783949

Gene: RP2

Linked Data

• dbSNP Id: rs1252874564
• gnomAD v3: X-46836939-A-G
• gnomAD v4: X-46836939-A-G
• MyVariant Identifiers: chrX:g.46836939A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.46836939A>G , CM000685.2:g.46836939A>G	GRCh38
NC_000023.10:g.46696374A>G , CM000685.1:g.46696374A>G	GRCh37
NC_000023.9:g.46581318A>G	NCBI36
NG_009107.1:g.5028A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006915.2:c.-162A>G	NP_008846.2:n.-162A>G