Canonical Allele Identifier: CA1907806002
Gene: RBP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47349987C= , CM000672.2:g.47349987C= GRCh38
NC_000010.10:g.48389375G= , CM000672.1:g.48389375G= GRCh37
NC_000010.9:g.48009381G= NCBI36
NG_029718.1:g.6617C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1503C= MANE Select ENSP00000463151.1:p.Ala501=
ENST00000584701.1:c.1503C= ENSP00000463151.1:p.Ala501=
NM_002900.2:c.1503C= NP_002891.1:p.Ala501=
NM_002900.3:c.1503C= MANE Select NP_002891.1:p.Ala501=