Canonical Allele Identifier: CA376671745
Gene: RBP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1002163
ClinVar RCV Id: RCV001298543
dbSNP Id: rs886047019
MyVariant Identifiers: chr10:g.48388959A>C (hg19) chr10:g.47350403T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47350403T>G , CM000672.2:g.47350403T>G GRCh38
NC_000010.10:g.48388959A>C , CM000672.1:g.48388959A>C GRCh37
NC_000010.9:g.48008965A>C NCBI36
NG_029718.1:g.7033T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1919T>G MANE Select ENSP00000463151.1:p.Val640Gly
ENST00000584701.1:c.1919T>G ENSP00000463151.1:p.Val640Gly
NM_002900.2:c.1919T>G NP_002891.1:p.Val640Gly
NM_002900.3:c.1919T>G MANE Select NP_002891.1:p.Val640Gly
Search 100 bp 5'
Search 100 bp 3'