Canonical Allele Identifier: CA469782543
Gene: RBP3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.48388835A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.47350527T>C , CM000672.2:g.47350527T>C GRCh38
NC_000010.10:g.48388835A>G , CM000672.1:g.48388835A>G GRCh37
NC_000010.9:g.48008841A>G NCBI36
NG_029718.1:g.7157T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000584701.2:c.2043T>C MANE Select ENSP00000463151.1:p.Ser681=
ENST00000584701.1:c.2043T>C ENSP00000463151.1:p.Ser681=
NM_002900.2:c.2043T>C NP_002891.1:p.Ser681=
NM_002900.3:c.2043T>C MANE Select NP_002891.1:p.Ser681=
Search 100 bp 5'
Search 100 bp 3'