Canonical Allele Identifier: CA206461805
Gene: RBP3 HGNC NCBI

Linked Data

dbSNP Id: rs782347332
gnomAD v4: 10-47349877-T-A
MyVariant Identifiers: chr10:g.48389485A>T (hg19) chr10:g.47349877T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47349877T>A , CM000672.2:g.47349877T>A GRCh38
NC_000010.10:g.48389485A>T , CM000672.1:g.48389485A>T GRCh37
NC_000010.9:g.48009491A>T NCBI36
NG_029718.1:g.6507T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1393T>A MANE Select ENSP00000463151.1:p.Trp465Arg
ENST00000584701.1:c.1393T>A ENSP00000463151.1:p.Trp465Arg
NM_002900.2:c.1393T>A NP_002891.1:p.Trp465Arg
NM_002900.3:c.1393T>A MANE Select NP_002891.1:p.Trp465Arg
Search 100 bp 5'
Search 100 bp 3'