Canonical Allele Identifier: CA469782455
Gene: RBP3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.48389159C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47350203G>A , CM000672.2:g.47350203G>A GRCh38
NC_000010.10:g.48389159C>T , CM000672.1:g.48389159C>T GRCh37
NC_000010.9:g.48009165C>T NCBI36
NG_029718.1:g.6833G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1719G>A MANE Select ENSP00000463151.1:p.Leu573=
ENST00000584701.1:c.1719G>A ENSP00000463151.1:p.Leu573=
NM_002900.2:c.1719G>A NP_002891.1:p.Leu573=
NM_002900.3:c.1719G>A MANE Select NP_002891.1:p.Leu573=