Canonical Allele Identifier: CA376676479
Gene: RBP3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.48385944A>G (hg19) chr10:g.47353418T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47353418T>C , CM000672.2:g.47353418T>C GRCh38
NC_000010.10:g.48385944A>G , CM000672.1:g.48385944A>G GRCh37
NC_000010.9:g.48005950A>G NCBI36
NG_029718.1:g.10048T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000584701.2:c.3148T>C MANE Select ENSP00000463151.1:p.Phe1050Leu
ENST00000584701.1:c.3148T>C ENSP00000463151.1:p.Phe1050Leu
NM_002900.2:c.3148T>C NP_002891.1:p.Phe1050Leu
NM_002900.3:c.3148T>C MANE Select NP_002891.1:p.Phe1050Leu
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