Canonical Allele Identifier: CA1907805901
Gene: RBP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47349897G= , CM000672.2:g.47349897G= GRCh38
NC_000010.10:g.48389465C= , CM000672.1:g.48389465C= GRCh37
NC_000010.9:g.48009471C= NCBI36
NG_029718.1:g.6527G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1413G= MANE Select ENSP00000463151.1:p.Thr471=
ENST00000584701.1:c.1413G= ENSP00000463151.1:p.Thr471=
NM_002900.2:c.1413G= NP_002891.1:p.Thr471=
NM_002900.3:c.1413G= MANE Select NP_002891.1:p.Thr471=