Canonical Allele Identifier: CA413039609
Gene: RP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.46713203C>A (hg19) chrX:g.46853768C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46853768C>A , CM000685.2:g.46853768C>A GRCh38
NC_000023.10:g.46713203C>A , CM000685.1:g.46713203C>A GRCh37
NC_000023.9:g.46598147C>A NCBI36
NG_009107.1:g.21857C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000218340.4:c.395C>A MANE Select ENSP00000218340.3:p.Ala132Asp
ENST00000218340.3:c.395C>A ENSP00000218340.3:p.Ala132Asp
NM_006915.2:c.395C>A NP_008846.2:p.Ala132Asp
NM_006915.3:c.395C>A MANE Select NP_008846.2:p.Ala132Asp
Search 100 bp 5'
Search 100 bp 3'