Canonical Allele Identifier: CA206461808
Gene: RBP3 HGNC NCBI

Linked Data

dbSNP Id: rs782195686
MyVariant Identifiers: chr10:g.48389479G>T (hg19) chr10:g.47349883C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47349883C>A , CM000672.2:g.47349883C>A GRCh38
NC_000010.10:g.48389479G>T , CM000672.1:g.48389479G>T GRCh37
NC_000010.9:g.48009485G>T NCBI36
NG_029718.1:g.6513C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1399C>A MANE Select ENSP00000463151.1:p.Pro467Thr
ENST00000584701.1:c.1399C>A ENSP00000463151.1:p.Pro467Thr
NM_002900.2:c.1399C>A NP_002891.1:p.Pro467Thr
NM_002900.3:c.1399C>A MANE Select NP_002891.1:p.Pro467Thr
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