Canonical Allele Identifier: CA376669718
Gene: RBP3 HGNC NCBI

Linked Data

dbSNP Id: rs1555211210
gnomAD v2: 10-48389460-T-C
gnomAD v4: 10-47349902-A-G
MyVariant Identifiers: chr10:g.48389460T>C (hg19) chr10:g.47349902A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47349902A>G , CM000672.2:g.47349902A>G GRCh38
NC_000010.10:g.48389460T>C , CM000672.1:g.48389460T>C GRCh37
NC_000010.9:g.48009466T>C NCBI36
NG_029718.1:g.6532A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.1418A>G MANE Select ENSP00000463151.1:p.His473Arg
ENST00000584701.1:c.1418A>G ENSP00000463151.1:p.His473Arg
NM_002900.2:c.1418A>G NP_002891.1:p.His473Arg
NM_002900.3:c.1418A>G MANE Select NP_002891.1:p.His473Arg
Search 100 bp 5'
Search 100 bp 3'