Canonical Allele Identifier: CA376676462
Gene: RBP3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.48385951A>T (hg19) chr10:g.47353411T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47353411T>A , CM000672.2:g.47353411T>A GRCh38
NC_000010.10:g.48385951A>T , CM000672.1:g.48385951A>T GRCh37
NC_000010.9:g.48005957A>T NCBI36
NG_029718.1:g.10041T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000584701.2:c.3141T>A MANE Select ENSP00000463151.1:p.Phe1047Leu
ENST00000584701.1:c.3141T>A ENSP00000463151.1:p.Phe1047Leu
NM_002900.2:c.3141T>A NP_002891.1:p.Phe1047Leu
NM_002900.3:c.3141T>A MANE Select NP_002891.1:p.Phe1047Leu
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