Canonical Allele Identifier: CA1907805834
Gene: RBP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47349853G= , CM000672.2:g.47349853G= GRCh38
NC_000010.10:g.48389509C= , CM000672.1:g.48389509C= GRCh37
NC_000010.9:g.48009515C= NCBI36
NG_029718.1:g.6483G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1369G= MANE Select ENSP00000463151.1:p.Ala457=
ENST00000584701.1:c.1369G= ENSP00000463151.1:p.Ala457=
NM_002900.2:c.1369G= NP_002891.1:p.Ala457=
NM_002900.3:c.1369G= MANE Select NP_002891.1:p.Ala457=