Canonical Allele Identifier: CA1907806729
Gene: RBP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47350613T= , CM000672.2:g.47350613T= GRCh38
NC_000010.10:g.48388749A= , CM000672.1:g.48388749A= GRCh37
NC_000010.9:g.48008755A= NCBI36
NG_029718.1:g.7243T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.2129T= MANE Select ENSP00000463151.1:p.Val710=
ENST00000584701.1:c.2129T= ENSP00000463151.1:p.Val710=
NM_002900.2:c.2129T= NP_002891.1:p.Val710=
NM_002900.3:c.2129T= MANE Select NP_002891.1:p.Val710=