Canonical Allele Identifier: CA1907809869
Gene: RBP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47353521T= , CM000672.2:g.47353521T= GRCh38
NC_000010.10:g.48385841A= , CM000672.1:g.48385841A= GRCh37
NC_000010.9:g.48005847A= NCBI36
NG_029718.1:g.10151T=

Transcript Alleles

HGVS Amino-acid change
ENST00000584701.2:c.3245+6T= MANE Select ENSP00000463151.1:n.3245+6T=
ENST00000584701.1:c.3245+6T= ENSP00000463151.1:n.3245+6T=
NM_002900.2:c.3245+6T= NP_002891.1:n.3245+6T=
NM_002900.3:c.3245+6T= MANE Select NP_002891.1:n.3245+6T=