Canonical Allele Identifier: CA5487349
Gene: RBP3 HGNC NCBI

Linked Data

dbSNP Id: rs141453777

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47350613T>A , CM000672.2:g.47350613T>A GRCh38
NC_000010.10:g.48388749A>T , CM000672.1:g.48388749A>T GRCh37
NC_000010.9:g.48008755A>T NCBI36
NG_029718.1:g.7243T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.2129T>A MANE Select ENSP00000463151.1:p.Val710Glu
ENST00000584701.1:c.2129T>A ENSP00000463151.1:p.Val710Glu
NM_002900.2:c.2129T>A NP_002891.1:p.Val710Glu
NM_002900.3:c.2129T>A MANE Select NP_002891.1:p.Val710Glu