Canonical Allele Identifier: CA376672078
Gene: RBP3 HGNC NCBI

Linked Data

dbSNP Id: rs2132254640

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47350589T>C , CM000672.2:g.47350589T>C GRCh38
NC_000010.10:g.48388773A>G , CM000672.1:g.48388773A>G GRCh37
NC_000010.9:g.48008779A>G NCBI36
NG_029718.1:g.7219T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.2105T>C MANE Select ENSP00000463151.1:p.Phe702Ser
ENST00000584701.1:c.2105T>C ENSP00000463151.1:p.Phe702Ser
NM_002900.2:c.2105T>C NP_002891.1:p.Phe702Ser
NM_002900.3:c.2105T>C MANE Select NP_002891.1:p.Phe702Ser