Canonical Allele Identifier: CA5487347
Gene: RBP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1402876
ClinVar RCV Id: RCV001897067
dbSNP Id: rs199522516

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47350624C>G , CM000672.2:g.47350624C>G GRCh38
NC_000010.10:g.48388738G>C , CM000672.1:g.48388738G>C GRCh37
NC_000010.9:g.48008744G>C NCBI36
NG_029718.1:g.7254C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.2140C>G MANE Select ENSP00000463151.1:p.Pro714Ala
ENST00000584701.1:c.2140C>G ENSP00000463151.1:p.Pro714Ala
NM_002900.2:c.2140C>G NP_002891.1:p.Pro714Ala
NM_002900.3:c.2140C>G MANE Select NP_002891.1:p.Pro714Ala