Canonical Allele Identifier: CA376676678
Gene: RBP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 999777
ClinVar RCV Id: RCV001295814
dbSNP Id: rs1395683742
MyVariant Identifiers: chr10:g.48385851T>C (hg19) chr10:g.47353511A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47353511A>G , CM000672.2:g.47353511A>G GRCh38
NC_000010.10:g.48385851T>C , CM000672.1:g.48385851T>C GRCh37
NC_000010.9:g.48005857T>C NCBI36
NG_029718.1:g.10141A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000584701.2:c.3241A>G MANE Select ENSP00000463151.1:p.Met1081Val
ENST00000584701.1:c.3241A>G ENSP00000463151.1:p.Met1081Val
NM_002900.2:c.3241A>G NP_002891.1:p.Met1081Val
NM_002900.3:c.3241A>G MANE Select NP_002891.1:p.Met1081Val
Search 100 bp 5'
Search 100 bp 3'