Canonical Allele Identifier: CA376672149
Gene: RBP3 HGNC NCBI

Linked Data

dbSNP Id: rs1299574313

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47350627C>T , CM000672.2:g.47350627C>T GRCh38
NC_000010.10:g.48388735G>A , CM000672.1:g.48388735G>A GRCh37
NC_000010.9:g.48008741G>A NCBI36
NG_029718.1:g.7257C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.2143C>T MANE Select ENSP00000463151.1:p.Pro715Ser
ENST00000584701.1:c.2143C>T ENSP00000463151.1:p.Pro715Ser
NM_002900.2:c.2143C>T NP_002891.1:p.Pro715Ser
NM_002900.3:c.2143C>T MANE Select NP_002891.1:p.Pro715Ser