Canonical Allele Identifier: CA413039182

Gene: RP2

Linked Data

• MyVariant Identifiers: chrX:g.46713086T>G (hg19) ; chrX:g.46853651T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.46853651T>G , CM000685.2:g.46853651T>G	GRCh38
NC_000023.10:g.46713086T>G , CM000685.1:g.46713086T>G	GRCh37
NC_000023.9:g.46598030T>G	NCBI36
NG_009107.1:g.21740T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218340.4:c.278T>G MANE Select	ENSP00000218340.3:p.Leu93Arg
ENST00000218340.3:c.278T>G	ENSP00000218340.3:p.Leu93Arg
NM_006915.2:c.278T>G	NP_008846.2:p.Leu93Arg
NM_006915.3:c.278T>G MANE Select	NP_008846.2:p.Leu93Arg