Canonical Allele Identifier: CA471368039
Gene: RBM20 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.112572057G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110812299G>A , CM000672.2:g.110812299G>A GRCh38
NC_000010.10:g.112572057G>A , CM000672.1:g.112572057G>A GRCh37
NC_000010.9:g.112562047G>A NCBI36
NG_021177.1:g.172903G>A , LRG_382:g.172903G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369519.4:c.1902G>A MANE Select ENSP00000358532.3:p.Arg634=
ENST00000369519.3:c.1902G>A ENSP00000358532.3:p.Arg634=
NM_001134363.2:c.1902G>A NP_001127835.2:p.Arg634=
XM_011539697.1:c.1518G>A XP_011537999.1:p.Arg506=
XM_017016103.2:c.1737G>A XP_016871592.1:p.Arg579=
XM_017016104.2:c.1518G>A XP_016871593.1:p.Arg506=
NM_001134363.3:c.1902G>A MANE Select NP_001127835.2:p.Arg634=
Search 100 bp 5'
Search 100 bp 3'