Canonical Allele Identifier: CA376671344

Gene: RBP3

Linked Data

• dbSNP Id: rs1588862626
• MyVariant Identifiers: chr10:g.48389173T>G (hg19) ; chr10:g.47350189A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.47350189A>C , CM000672.2:g.47350189A>C	GRCh38
NC_000010.10:g.48389173T>G , CM000672.1:g.48389173T>G	GRCh37
NC_000010.9:g.48009179T>G	NCBI36
NG_029718.1:g.6819A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584701.2:c.1705A>C MANE Select	ENSP00000463151.1:p.Thr569Pro
ENST00000584701.1:c.1705A>C	ENSP00000463151.1:p.Thr569Pro
NM_002900.2:c.1705A>C	NP_002891.1:p.Thr569Pro
NM_002900.3:c.1705A>C MANE Select	NP_002891.1:p.Thr569Pro