Canonical Allele Identifier: CA469782392
Gene: RBP3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.48388730T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47350632A>G , CM000672.2:g.47350632A>G GRCh38
NC_000010.10:g.48388730T>C , CM000672.1:g.48388730T>C GRCh37
NC_000010.9:g.48008736T>C NCBI36
NG_029718.1:g.7262A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.2148A>G MANE Select ENSP00000463151.1:p.Pro716=
ENST00000584701.1:c.2148A>G ENSP00000463151.1:p.Pro716=
NM_002900.2:c.2148A>G NP_002891.1:p.Pro716=
NM_002900.3:c.2148A>G MANE Select NP_002891.1:p.Pro716=
Search 100 bp 5'
Search 100 bp 3'