Canonical Allele Identifier: CA1907806683
Gene: RBP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47350591C= , CM000672.2:g.47350591C= GRCh38
NC_000010.10:g.48388771G= , CM000672.1:g.48388771G= GRCh37
NC_000010.9:g.48008777G= NCBI36
NG_029718.1:g.7221C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.2107C= MANE Select ENSP00000463151.1:p.His703=
ENST00000584701.1:c.2107C= ENSP00000463151.1:p.His703=
NM_002900.2:c.2107C= NP_002891.1:p.His703=
NM_002900.3:c.2107C= MANE Select NP_002891.1:p.His703=