Canonical Allele Identifier: CA5487421
Gene: RBP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 299976
dbSNP Id: rs34044042

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47350293C>T , CM000672.2:g.47350293C>T GRCh38
NC_000010.10:g.48389069G>A , CM000672.1:g.48389069G>A GRCh37
NC_000010.9:g.48009075G>A NCBI36
NG_029718.1:g.6923C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1809C>T MANE Select ENSP00000463151.1:p.Gly603=
ENST00000584701.1:c.1809C>T ENSP00000463151.1:p.Gly603=
NM_002900.2:c.1809C>T NP_002891.1:p.Gly603=
NM_002900.3:c.1809C>T MANE Select NP_002891.1:p.Gly603=