Canonical Allele Identifier: CA1907806051
Gene: RBP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47350022G= , CM000672.2:g.47350022G= GRCh38
NC_000010.10:g.48389340C= , CM000672.1:g.48389340C= GRCh37
NC_000010.9:g.48009346C= NCBI36
NG_029718.1:g.6652G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1538G= MANE Select ENSP00000463151.1:p.Arg513=
ENST00000584701.1:c.1538G= ENSP00000463151.1:p.Arg513=
NM_002900.2:c.1538G= NP_002891.1:p.Arg513=
NM_002900.3:c.1538G= MANE Select NP_002891.1:p.Arg513=