Canonical Allele Identifier: CA1907806018
Gene: RBP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47349998A= , CM000672.2:g.47349998A= GRCh38
NC_000010.10:g.48389364T= , CM000672.1:g.48389364T= GRCh37
NC_000010.9:g.48009370T= NCBI36
NG_029718.1:g.6628A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1514A= MANE Select ENSP00000463151.1:p.His505=
ENST00000584701.1:c.1514A= ENSP00000463151.1:p.His505=
NM_002900.2:c.1514A= NP_002891.1:p.His505=
NM_002900.3:c.1514A= MANE Select NP_002891.1:p.His505=