Canonical Allele Identifier: CA350950
Gene: RBP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 208320
ClinVar RCV Id: RCV000206948
dbSNP Id: rs373766942
MyVariant Identifiers: chr10:g.48388170G>C (hg19) chr10:g.47351192C>G (hg38)
PubMed: PMID:19074801
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47351192C>G , CM000672.2:g.47351192C>G GRCh38
NC_000010.10:g.48388170G>C , CM000672.1:g.48388170G>C GRCh37
NC_000010.9:g.48008176G>C NCBI36
NG_029718.1:g.7822C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.2708C>G MANE Select ENSP00000463151.1:p.Thr903Arg
ENST00000584701.1:c.2708C>G ENSP00000463151.1:p.Thr903Arg
NM_002900.2:c.2708C>G NP_002891.1:p.Thr903Arg
NM_002900.3:c.2708C>G MANE Select NP_002891.1:p.Thr903Arg
Search 100 bp 5'
Search 100 bp 3'