Canonical Allele Identifier: CA376670112
Gene: RBP3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.48389363G>T (hg19) chr10:g.47349999C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47349999C>A , CM000672.2:g.47349999C>A GRCh38
NC_000010.10:g.48389363G>T , CM000672.1:g.48389363G>T GRCh37
NC_000010.9:g.48009369G>T NCBI36
NG_029718.1:g.6629C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1515C>A MANE Select ENSP00000463151.1:p.His505Gln
ENST00000584701.1:c.1515C>A ENSP00000463151.1:p.His505Gln
NM_002900.2:c.1515C>A NP_002891.1:p.His505Gln
NM_002900.3:c.1515C>A MANE Select NP_002891.1:p.His505Gln
Search 100 bp 5'
Search 100 bp 3'