Canonical Allele Identifier: CA2427726107

Gene: RP2

Linked Data

• dbSNP Id: rs1924508648
• gnomAD v4: X-46836917-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.46836917G>T , CM000685.2:g.46836917G>T	GRCh38
NC_000023.10:g.46696352G>T , CM000685.1:g.46696352G>T	GRCh37
NC_000023.9:g.46581296G>T	NCBI36
NG_009107.1:g.5006G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006915.2:c.-184G>T	NP_008846.2:n.-184G>T