Canonical Allele Identifier: CA206461952
Gene: RBP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 3028170
ClinVar RCV Id: RCV003889540
gnomAD v4: 10-47349986-C-A
MyVariant Identifiers: chr10:g.48389376G>T (hg19) chr10:g.47349986C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47349986C>A , CM000672.2:g.47349986C>A GRCh38
NC_000010.10:g.48389376G>T , CM000672.1:g.48389376G>T GRCh37
NC_000010.9:g.48009382G>T NCBI36
NG_029718.1:g.6616C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1502C>A MANE Select ENSP00000463151.1:p.Ala501Asp
ENST00000584701.1:c.1502C>A ENSP00000463151.1:p.Ala501Asp
NM_002900.2:c.1502C>A NP_002891.1:p.Ala501Asp
NM_002900.3:c.1502C>A MANE Select NP_002891.1:p.Ala501Asp
Search 100 bp 5'
Search 100 bp 3'