Canonical Allele Identifier: CA376671400
Gene: RBP3 HGNC NCBI

Linked Data

dbSNP Id: rs1169208510

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47350216A>T , CM000672.2:g.47350216A>T GRCh38
NC_000010.10:g.48389146T>A , CM000672.1:g.48389146T>A GRCh37
NC_000010.9:g.48009152T>A NCBI36
NG_029718.1:g.6846A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1732A>T MANE Select ENSP00000463151.1:p.Thr578Ser
ENST00000584701.1:c.1732A>T ENSP00000463151.1:p.Thr578Ser
NM_002900.2:c.1732A>T NP_002891.1:p.Thr578Ser
NM_002900.3:c.1732A>T MANE Select NP_002891.1:p.Thr578Ser