Canonical Allele Identifier: CA875783946

Gene: RP2

Linked Data

• dbSNP Id: rs1195866320
• gnomAD v3: X-46836929-A-G
• gnomAD v4: X-46836929-A-G
• MyVariant Identifiers: chrX:g.46836929A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_006915.2:c.-172A>G	NP_008846.2:n.-172A>G