Canonical Allele Identifier: CA469781461
Gene: RBP3 HGNC NCBI

Linked Data

dbSNP Id: rs1555211199
MyVariant Identifiers: chr10:g.48389504_48389505insG (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47349857dup , CM000672.2:g.47349857dup GRCh38
NC_000010.10:g.48389508dup , CM000672.1:g.48389508dup GRCh37
NC_000010.9:g.48009514dup NCBI36
NG_029718.1:g.6487dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1373dup MANE Select ENSP00000463151.1:p.Tyr459IlefsTer?
ENST00000584701.1:c.1373dup ENSP00000463151.1:p.Tyr459IlefsTer?
NM_002900.2:c.1373dup NP_002891.1:p.Tyr459IlefsTer?
NM_002900.3:c.1373dup MANE Select NP_002891.1:p.Tyr459IlefsTer?
Search 100 bp 5'
Search 100 bp 3'