Canonical Allele Identifier: CA1907805863
Gene: RBP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47349877T= , CM000672.2:g.47349877T= GRCh38
NC_000010.10:g.48389485A= , CM000672.1:g.48389485A= GRCh37
NC_000010.9:g.48009491A= NCBI36
NG_029718.1:g.6507T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1393T= MANE Select ENSP00000463151.1:p.Trp465=
ENST00000584701.1:c.1393T= ENSP00000463151.1:p.Trp465=
NM_002900.2:c.1393T= NP_002891.1:p.Trp465=
NM_002900.3:c.1393T= MANE Select NP_002891.1:p.Trp465=