Canonical Allele Identifier: CA376672012
Gene: RBP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1052314
ClinVar RCV Id: RCV001360471 RCV002550009
dbSNP Id: rs1555211402
gnomAD v2: 10-48388811-G-T
gnomAD v4: 10-47350551-C-A
MyVariant Identifiers: chr10:g.48388811G>T (hg19) chr10:g.47350551C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47350551C>A , CM000672.2:g.47350551C>A GRCh38
NC_000010.10:g.48388811G>T , CM000672.1:g.48388811G>T GRCh37
NC_000010.9:g.48008817G>T NCBI36
NG_029718.1:g.7181C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.2067C>A MANE Select ENSP00000463151.1:p.Asp689Glu
ENST00000584701.1:c.2067C>A ENSP00000463151.1:p.Asp689Glu
NM_002900.2:c.2067C>A NP_002891.1:p.Asp689Glu
NM_002900.3:c.2067C>A MANE Select NP_002891.1:p.Asp689Glu
Search 100 bp 5'
Search 100 bp 3'