Canonical Allele Identifier: CA469781557
Gene: RBP3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.48389351_48389353del (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47350009_47350011del , CM000672.2:g.47350009_47350011del GRCh38
NC_000010.10:g.48389355_48389357del , CM000672.1:g.48389355_48389357del GRCh37
NC_000010.9:g.48009361_48009363del NCBI36
NG_029718.1:g.6639_6641del

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1525_1527del MANE Select ENSP00000463151.1:p.Thr509del
ENST00000584701.1:c.1525_1527del ENSP00000463151.1:p.Thr509del
NM_002900.2:c.1525_1527del NP_002891.1:p.Thr509del
NM_002900.3:c.1525_1527del MANE Select NP_002891.1:p.Thr509del
Search 100 bp 5'
Search 100 bp 3'