Canonical Allele Identifier: CA875783980

Gene: RP2

Linked Data

• dbSNP Id: rs1175952573
• gnomAD v3: X-46836981-TG-T
• gnomAD v4: X-46836981-TG-T
• MyVariant Identifiers: chrX:g.46836982del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.46836984del , CM000685.2:g.46836984del	GRCh38
NC_000023.10:g.46696419del , CM000685.1:g.46696419del	GRCh37
NC_000023.9:g.46581363del	NCBI36
NG_009107.1:g.5073del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218340.3:c.-117del	ENSP00000218340.3:n.-117del
NM_006915.2:c.-117del	NP_008846.2:n.-117del