Canonical Allele Identifier: CA1907809752
Gene: RBP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47353423G= , CM000672.2:g.47353423G= GRCh38
NC_000010.10:g.48385939C= , CM000672.1:g.48385939C= GRCh37
NC_000010.9:g.48005945C= NCBI36
NG_029718.1:g.10053G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.3153G= MANE Select ENSP00000463151.1:p.Gly1051=
ENST00000584701.1:c.3153G= ENSP00000463151.1:p.Gly1051=
NM_002900.2:c.3153G= NP_002891.1:p.Gly1051=
NM_002900.3:c.3153G= MANE Select NP_002891.1:p.Gly1051=