Canonical Allele Identifier: CA469782398
Gene: RBP3 HGNC NCBI

Linked Data

dbSNP Id: rs1229836742
MyVariant Identifiers: chr10:g.48388727G>A (hg19) chr10:g.47350635C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47350635C>T , CM000672.2:g.47350635C>T GRCh38
NC_000010.10:g.48388727G>A , CM000672.1:g.48388727G>A GRCh37
NC_000010.9:g.48008733G>A NCBI36
NG_029718.1:g.7265C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.2151C>T MANE Select ENSP00000463151.1:p.Pro717=
ENST00000584701.1:c.2151C>T ENSP00000463151.1:p.Pro717=
NM_002900.2:c.2151C>T NP_002891.1:p.Pro717=
NM_002900.3:c.2151C>T MANE Select NP_002891.1:p.Pro717=
Search 100 bp 5'
Search 100 bp 3'