Canonical Allele Identifier: CA206466910
Gene: RBP3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.48385997G>T (hg19) chr10:g.47353365C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47353365C>A , CM000672.2:g.47353365C>A GRCh38
NC_000010.10:g.48385997G>T , CM000672.1:g.48385997G>T GRCh37
NC_000010.9:g.48006003G>T NCBI36
NG_029718.1:g.9995C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.3095C>A MANE Select ENSP00000463151.1:p.Ser1032Tyr
ENST00000584701.1:c.3095C>A ENSP00000463151.1:p.Ser1032Tyr
NM_002900.2:c.3095C>A NP_002891.1:p.Ser1032Tyr
NM_002900.3:c.3095C>A MANE Select NP_002891.1:p.Ser1032Tyr
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