Canonical Allele Identifier: CA376670119

Gene: RBP3

Linked Data

• MyVariant Identifiers: chr10:g.48389361A>T (hg19) ; chr10:g.47350001T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.47350001T>A , CM000672.2:g.47350001T>A	GRCh38
NC_000010.10:g.48389361A>T , CM000672.1:g.48389361A>T	GRCh37
NC_000010.9:g.48009367A>T	NCBI36
NG_029718.1:g.6631T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584701.2:c.1517T>A MANE Select	ENSP00000463151.1:p.Leu506His
ENST00000584701.1:c.1517T>A	ENSP00000463151.1:p.Leu506His
NM_002900.2:c.1517T>A	NP_002891.1:p.Leu506His
NM_002900.3:c.1517T>A MANE Select	NP_002891.1:p.Leu506His