Canonical Allele Identifier: CA206467047
Gene: RBP3 HGNC NCBI

Linked Data

dbSNP Id: rs140160521
MyVariant Identifiers: chr10:g.48385935C>A (hg19) chr10:g.47353427G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47353427G>T , CM000672.2:g.47353427G>T GRCh38
NC_000010.10:g.48385935C>A , CM000672.1:g.48385935C>A GRCh37
NC_000010.9:g.48005941C>A NCBI36
NG_029718.1:g.10057G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000584701.2:c.3157G>T MANE Select ENSP00000463151.1:p.Gly1053Cys
ENST00000584701.1:c.3157G>T ENSP00000463151.1:p.Gly1053Cys
NM_002900.2:c.3157G>T NP_002891.1:p.Gly1053Cys
NM_002900.3:c.3157G>T MANE Select NP_002891.1:p.Gly1053Cys
Search 100 bp 5'
Search 100 bp 3'