Canonical Allele Identifier: CA516371021
Gene: RP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.46713207T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.46853772T>C , CM000685.2:g.46853772T>C GRCh38
NC_000023.10:g.46713207T>C , CM000685.1:g.46713207T>C GRCh37
NC_000023.9:g.46598151T>C NCBI36
NG_009107.1:g.21861T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000218340.4:c.399T>C MANE Select ENSP00000218340.3:p.Thr133=
ENST00000218340.3:c.399T>C ENSP00000218340.3:p.Thr133=
NM_006915.2:c.399T>C NP_008846.2:p.Thr133=
NM_006915.3:c.399T>C MANE Select NP_008846.2:p.Thr133=
Search 100 bp 5'
Search 100 bp 3'