Canonical Allele Identifier: CA376669802
Gene: RBP3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.48389439T>G (hg19) chr10:g.47349923A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47349923A>C , CM000672.2:g.47349923A>C GRCh38
NC_000010.10:g.48389439T>G , CM000672.1:g.48389439T>G GRCh37
NC_000010.9:g.48009445T>G NCBI36
NG_029718.1:g.6553A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1439A>C MANE Select ENSP00000463151.1:p.His480Pro
ENST00000584701.1:c.1439A>C ENSP00000463151.1:p.His480Pro
NM_002900.2:c.1439A>C NP_002891.1:p.His480Pro
NM_002900.3:c.1439A>C MANE Select NP_002891.1:p.His480Pro
Search 100 bp 5'
Search 100 bp 3'