Canonical Allele Identifier: CA376670003

Gene: RBP3

Linked Data

• MyVariant Identifiers: chr10:g.48389391A>C (hg19) ; chr10:g.47349971T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.47349971T>G , CM000672.2:g.47349971T>G	GRCh38
NC_000010.10:g.48389391A>C , CM000672.1:g.48389391A>C	GRCh37
NC_000010.9:g.48009397A>C	NCBI36
NG_029718.1:g.6601T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584701.2:c.1487T>G MANE Select	ENSP00000463151.1:p.Phe496Cys
ENST00000584701.1:c.1487T>G	ENSP00000463151.1:p.Phe496Cys
NM_002900.2:c.1487T>G	NP_002891.1:p.Phe496Cys
NM_002900.3:c.1487T>G MANE Select	NP_002891.1:p.Phe496Cys