Canonical Allele Identifier: CA413039174
Gene: RP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.46713083T>A (hg19) chrX:g.46853648T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46853648T>A , CM000685.2:g.46853648T>A GRCh38
NC_000023.10:g.46713083T>A , CM000685.1:g.46713083T>A GRCh37
NC_000023.9:g.46598027T>A NCBI36
NG_009107.1:g.21737T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000218340.4:c.275T>A MANE Select ENSP00000218340.3:p.Phe92Tyr
ENST00000218340.3:c.275T>A ENSP00000218340.3:p.Phe92Tyr
NM_006915.2:c.275T>A NP_008846.2:p.Phe92Tyr
NM_006915.3:c.275T>A MANE Select NP_008846.2:p.Phe92Tyr
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