Canonical Allele Identifier: CA206462034
Gene: RBP3 HGNC NCBI

Linked Data

dbSNP Id: rs782133131
MyVariant Identifiers: chr10:g.48389329T>G (hg19) chr10:g.47350033A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47350033A>C , CM000672.2:g.47350033A>C GRCh38
NC_000010.10:g.48389329T>G , CM000672.1:g.48389329T>G GRCh37
NC_000010.9:g.48009335T>G NCBI36
NG_029718.1:g.6663A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1549A>C MANE Select ENSP00000463151.1:p.Thr517Pro
ENST00000584701.1:c.1549A>C ENSP00000463151.1:p.Thr517Pro
NM_002900.2:c.1549A>C NP_002891.1:p.Thr517Pro
NM_002900.3:c.1549A>C MANE Select NP_002891.1:p.Thr517Pro
Search 100 bp 5'
Search 100 bp 3'