Canonical Allele Identifier: CA1907805842
Gene: RBP3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47349861T= , CM000672.2:g.47349861T= GRCh38
NC_000010.10:g.48389501A= , CM000672.1:g.48389501A= GRCh37
NC_000010.9:g.48009507A= NCBI36
NG_029718.1:g.6491T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1377T= MANE Select ENSP00000463151.1:p.Tyr459=
ENST00000584701.1:c.1377T= ENSP00000463151.1:p.Tyr459=
NM_002900.2:c.1377T= NP_002891.1:p.Tyr459=
NM_002900.3:c.1377T= MANE Select NP_002891.1:p.Tyr459=
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