Canonical Allele Identifier: CA469781498
Gene: RBP3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.48389444C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47349918G>T , CM000672.2:g.47349918G>T GRCh38
NC_000010.10:g.48389444C>A , CM000672.1:g.48389444C>A GRCh37
NC_000010.9:g.48009450C>A NCBI36
NG_029718.1:g.6548G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1434G>T MANE Select ENSP00000463151.1:p.Leu478=
ENST00000584701.1:c.1434G>T ENSP00000463151.1:p.Leu478=
NM_002900.2:c.1434G>T NP_002891.1:p.Leu478=
NM_002900.3:c.1434G>T MANE Select NP_002891.1:p.Leu478=
Search 100 bp 5'
Search 100 bp 3'