Canonical Allele Identifier: CA413039169

Gene: RP2

Linked Data

• MyVariant Identifiers: chrX:g.46713081T>G (hg19) ; chrX:g.46853646T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.46853646T>G , CM000685.2:g.46853646T>G	GRCh38
NC_000023.10:g.46713081T>G , CM000685.1:g.46713081T>G	GRCh37
NC_000023.9:g.46598025T>G	NCBI36
NG_009107.1:g.21735T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218340.4:c.273T>G MANE Select	ENSP00000218340.3:p.Ile91Met
ENST00000218340.3:c.273T>G	ENSP00000218340.3:p.Ile91Met
NM_006915.2:c.273T>G	NP_008846.2:p.Ile91Met
NM_006915.3:c.273T>G MANE Select	NP_008846.2:p.Ile91Met